Hetero Drugs
NDC Database
Hetero Drugs
NDC Database
National Drug Code (NDC) records including drug products, NDC numbers, nonproprietary names, dosage forms, strengths, labelers and marketing information.
- Total Records 162
- Latest Marketing Date 2025-06-10
- Data Source FDA
- First Marketing Date 1953-01-15
Company Overview
Social Profiles
Company Snapshot
Hetero Drugs
7-2-A2, Hetero Corporate Industrial Estates, Sanath Nagar Hyderabad,Telangana
India
www.hetero.com/ contact@heterodrugs.com View on MapNDC Records ( 162 records )
Nonproprietary Name
Bicalutamide (Form-H1)
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
BICALUTAMIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1995-10-04
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Terbinafine Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
TERBINAFINE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1992-12-30
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Ramipril
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
RAMIPRIL
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1991-01-28
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Irbesartan
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
IRBESARTAN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1997-09-30
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Levetiracetam (Form-I)
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
LEVETIRACETAM
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1999-11-30
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Escitalopram Oxalate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
ESCITALOPRAM OXALATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2002-08-14
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Losartan Potassium
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
LOSARTAN POTASSIUM
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1995-04-14
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Zonisamide
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
ZONISAMIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2003-08-22
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Simvastatin
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
SIMVASTATIN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1991-12-23
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Thalidomide
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
THALIDOMIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1998-07-16
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Nevirapine Anhydrous
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
NEVIRAPINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1996-06-21
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Lamivudine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
LAMIVUDINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1995-11-17
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Zidovudine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
ZIDOVUDINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1987-03-19
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Efavirenz
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
EFAVIRENZ
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1998-09-17
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Lopinavir
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
LOPINAVIR
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2000-09-15
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Aripiprazole
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
ARIPIPRAZOLE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2002-11-15
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Atomoxetine Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
ATOMOXETINE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2002-11-26
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Finasteride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
FINASTERIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1992-06-19
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Hydralazine Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
HYDRALAZINE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1982-01-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Quetiapine Fumarate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
QUETIAPINE FUMARATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1997-09-26
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Torsemide
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
TORSEMIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1993-08-23
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Anastrozole
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
ANASTROZOLE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1995-12-27
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Emtricitabine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
EMTRICITABINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2003-07-02
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Gemcitabine Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
GEMCITABINE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1996-05-15
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Oseltamivir Phosphate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
OSELTAMIVIR PHOSPHATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2007-07-02
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Pioglitazone Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
PIOGLITAZONE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1999-07-15
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Tenofovir Disoproxil Fumarate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
TENOFOVIR DISOPROXIL FUMARATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2012-01-18
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Abacavir Sulfate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
ABACAVIR SULFATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1998-12-17
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Capecitabine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
CAPECITABINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1998-04-30
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Imatinib
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
IMATINIB MESYLATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2003-05-18
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Darunavir
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
DARUNAVIR
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2006-06-23
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Saquinavir
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
SAQUINAVIR MESYLATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1995-12-06
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Zoledronic Acid
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
ZOLEDRONIC ACID
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1995-12-06
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Letrozole
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
LETROZOLE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1997-07-25
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Maraviroc
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
MARAVIROC
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2007-08-06
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Valsartan
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
VALSARTAN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1998-03-06
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Efavirenz
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
EFAVIRENZ
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1998-09-17
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Lamivudine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
LAMIVUDINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1995-11-17
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Nevirapine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
NEVIRAPINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1998-09-11
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Tenofovir Disoproxil
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
TENOFOVIR DISOPROXIL FUMARATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2001-10-26
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Zidovudine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
ZIDOVUDINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1987-03-19
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Temozolomide
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
TEMOZOLOMIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1999-08-11
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Bendamustine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
BENDAMUSTINE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2012-12-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Bortezomib
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
BORTEZOMIB
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2003-05-13
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Erlotinib
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
ERLOTINIB HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2004-11-18
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Etoricoxib
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
ETORICOXIB
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2012-12-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Irinotecan
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
IRINOTECAN HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1996-06-14
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Atazanavir Sulfate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
ATAZANAVIR SULFATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2003-06-20
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Etravirine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
ETRAVIRINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2008-01-18
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Pazopanib Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
PAZOPANIB HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2009-10-19
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Nilotinib Hydrochloride Dihydrate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
NILOTINIB HYDROCHLORIDE DIHYDRATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2014-01-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Gefitinib
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
GEFITINIB
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2014-01-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Paclitaxel
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
PACLITAXEL
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2005-01-07
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Cyclophosphamide
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
CYCLOPHOSPHAMIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1982-01-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Abacavir Sulfate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
ABACAVIR SULFATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1998-12-17
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Emtricitabine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
EMTRICITABINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2003-07-02
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Levetiracetam
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
LEVETIRACETAM
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2006-07-31
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Milnacipran Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
MILNACIPRAN HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2009-01-14
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Plerixafor
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
PLERIXAFOR
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2008-12-15
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Entacapone
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
ENTACAPONE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1999-10-19
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Olmesartan Medoxomil
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
OLMESARTAN MEDOXOMIL
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2010-07-23
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Dasatinib
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
DASATINIB
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2006-06-28
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Pralatrexate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
PRALATREXATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2009-09-24
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Lapatinib Ditosylate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
LAPATINIB DITOSYLATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2007-03-13
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Sorafenib
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
SORAFENIB TOSYLATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2005-12-20
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
PEMETREXED DISODIUM HEMIPENTAHYDRATE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
PEMETREXED DISODIUM HEMIPENTAHYDRATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2004-02-04
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Cisplatin
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
CISPLATIN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2000-05-16
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Sunitinib Malate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
SUNITINIB MALATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2006-01-26
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Dutasteride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
DUTASTERIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2001-11-20
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Cabazitaxel
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
CABAZITAXEL
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2010-06-17
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Bexarotene
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
BEXAROTENE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1999-12-29
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Abiraterone Acetate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
ABIRATERONE ACETATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2011-04-28
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Oxaliplatin
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
OXALIPLATIN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2005-01-31
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Carboplatin
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
CARBOPLATIN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2004-10-15
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Ezetimibe
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
EZETIMIBE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2013-05-03
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Melphalan Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
MELPHALAN HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1992-11-18
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Quetiapine Fumarate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
QUETIAPINE FUMARATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2001-05-17
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Lenalidomide
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
LENALIDOMIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2005-12-27
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Pomalidomide
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
POMALIDOMIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2013-02-08
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
pomalidomide
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
REGORAFENIB ANHYDROUS
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2012-09-27
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Dolutegravir Sodium
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
DOLUTEGRAVIR SODIUM
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2013-08-12
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Daclatasvir Dihydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
DACLATASVIR DIHYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2015-07-24
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Atorvastatin Calcium Trihydrate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
ATORVASTATIN CALCIUM TRIHYDRATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1996-12-17
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Atazanavir Sulfate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
ATAZANAVIR SULFATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2014-06-02
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Azacitidine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
AZACITIDINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2016-04-29
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Tenofovir Alafenamide Hemifumarate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
TENOFOVIR ALAFENAMIDE FUMARATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2016-03-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Enzalutamide
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
ENZALUTAMIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2012-08-31
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Afatinib Dimaleate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
AFATINIB DIMALEATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2013-07-12
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Ibrutinib
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
IBRUTINIB
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2013-11-13
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Vortioxetine Hydrobromide
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
VORTIOXETINE HYDROBROMIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2013-09-30
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Voriconazole
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
VORICONAZOLE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2003-12-19
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Palbociclib
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
PALBOCICLIB
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2015-02-03
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Darunavir
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
DARUNAVIR
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2020-01-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Levomilnacipran
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
LEVOMILNACIPRAN HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2013-07-25
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Eplerenone
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
EPLERENONE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2002-09-27
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Ritonavir
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
RITONAVIR
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1996-03-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Tipiracil Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
TIPIRACIL HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2015-09-22
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Olaparib
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
OLAPARIB
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2014-12-19
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
OBETICHOLIC ACID
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
OBETICHOLIC ACID
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2016-05-27
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
BICTEGRAVIR SODIUM
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
BICTEGRAVIR
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2018-02-07
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Nintedanib esylate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
NINTEDANIB ESYLATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2014-10-15
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Etravirine Premix
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
ETRAVIRINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2012-03-26
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Midostaurin
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
MIDOSTAURIN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-04-28
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Apalutamide
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
APALUTAMIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2018-02-14
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Gabapentin
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HETERO LABS LIMITED
Marketing Category
BULK INGREDIENT
Substance
GABAPENTIN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1993-12-30
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Naproxen Sodium
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
NAPROXEN SODIUM
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1994-11-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Fostamatinib Disodium Hexahydrate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HETERO LABS LIMITED
Marketing Category
BULK INGREDIENT
Substance
FOSTAMATINIB DISODIUM
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2018-04-17
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Elagolix Sodium
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HETERO LABS LIMITED
Marketing Category
BULK INGREDIENT
Substance
ELAGOLIX SODIUM
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2018-07-23
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
DORAVIRINE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HETERO LABS LIMITED
Marketing Category
BULK INGREDIENT
Substance
DORAVIRINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2018-08-30
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Doravirine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HETERO LABS LIMITED
Marketing Category
BULK INGREDIENT
Substance
DORAVIRINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2018-08-30
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Dolutegravir
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HETERO LABS LIMITED
Marketing Category
BULK INGREDIENT
Substance
DOLUTEGRAVIR SODIUM
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2016-06-09
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Escitalopram Oxalate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HETERO LABS LIMITED
Marketing Category
BULK INGREDIENT
Substance
ESCITALOPRAM OXALATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2002-08-14
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Etravirine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
ETRAVIRINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2010-12-22
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Lopinavir
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
LOPINAVIR
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2005-10-28
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Sofosbuvir
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
SOFOSBUVIR
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2013-12-06
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Darolutamide Premix
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HETERO LABS LIMITED
Marketing Category
BULK INGREDIENT
Substance
DAROLUTAMIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2019-07-30
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Vemlidy
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
TENOFOVIR ALAFENAMIDE FUMARATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2016-11-10
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Tolvaptan Povidone Premix
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HETERO LABS LIMITED
Marketing Category
BULK INGREDIENT
Substance
TOLVAPTAN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2018-04-23
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Naproxen
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HETERO LABS LIMITED
Marketing Category
BULK INGREDIENT
Substance
NAPROXEN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1994-10-14
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Tenofovir Alafenamide Hemifumarate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HETERO LABS LIMITED
Marketing Category
BULK INGREDIENT
Substance
TENOFOVIR ALAFENAMIDE FUMARATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2016-03-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Pregabalin
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HETERO LABS LIMITED
Marketing Category
BULK INGREDIENT
Substance
PREGABALIN
Product Type
BULK INGREDIENT
DEA Schedule
CV
Start Marketing Date
2004-12-30
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Hydroxy Chloroquine Sulfate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HETERO LABS LIMITED
Marketing Category
BULK INGREDIENT
Substance
HYDROXYCHLOROQUINE SULFATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1955-04-18
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Escitalopram Oxalate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HETERO LABS LIMITED
Marketing Category
BULK INGREDIENT
Substance
ESCITALOPRAM OXALATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2002-08-14
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Hydralazine Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HETERO LABS LIMITED
Marketing Category
BULK INGREDIENT
Substance
HYDRALAZINE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1953-01-15
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Atomoxetine Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HETERO LABS LIMITED
Marketing Category
BULK INGREDIENT
Substance
ATOMOXETINE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2002-11-26
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Alectinib Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HETERO LABS LIMITED
Marketing Category
BULK INGREDIENT
Substance
ALECTINIB HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2015-12-11
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Vortioxetine Hydrobromide
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HETERO LABS LIMITED
Marketing Category
BULK INGREDIENT
Substance
VORTIOXETINE HYDROBROMIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2013-09-30
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Ezetimibe
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HETERO LABS LIMITED
Marketing Category
BULK INGREDIENT
Substance
EZETIMIBE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2013-05-03
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Lidocaine Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HETERO LABS LIMITED
Marketing Category
BULK INGREDIENT
Substance
LIDOCAINE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1982-01-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Fostamatinib Disodium Hexahydrate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HETERO LABS LIMITED
Marketing Category
BULK INGREDIENT
Substance
FOSTAMATINIB DISODIUM
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2018-04-17
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Elagolix Sodium
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HETERO LABS LIMITED
Marketing Category
BULK INGREDIENT
Substance
ELAGOLIX SODIUM
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2018-07-23
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Pioglitazone Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HETERO LABS LIMITED
Marketing Category
BULK INGREDIENT
Substance
PIOGLITAZONE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1999-07-15
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Diltiazem Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HETERO LABS LIMITED
Marketing Category
BULK INGREDIENT
Substance
DILTIAZEM HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1982-11-05
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Maraviroc
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HETERO LABS LIMITED
Marketing Category
BULK INGREDIENT
Substance
MARAVIROC
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-08-06
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Acyclovir
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HETERO LABS LIMITED
Marketing Category
BULK INGREDIENT
Substance
ACYCLOVIR
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1982-03-29
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Lenvatinib
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HETERO LABS LIMITED
Marketing Category
BULK INGREDIENT
Substance
LENVATINIB
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2015-02-13
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Bosutinib
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HETERO LABS LIMITED
Marketing Category
BULK INGREDIENT
Substance
BOSUTINIB
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2023-09-26
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Venetoclax
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HETERO LABS LIMITED
Marketing Category
BULK INGREDIENT
Substance
VENETOCLAX
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2016-04-11
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Carfilzomib
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HETERO LABS LIMITED
Marketing Category
BULK INGREDIENT
Substance
CARFILZOMIB
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2019-09-09
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Vericiguat
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HETERO LABS LIMITED
Marketing Category
BULK INGREDIENT
Substance
VERICIGUAT
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2021-01-19
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Relugolix (Form-I)
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
RELUGOLIX
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2020-12-18
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Trilaciclib Dihydrochloride Dihydrate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HETERO LABS LIMITED
Marketing Category
BULK INGREDIENT
Substance
TRILACICLIB DIHYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2021-02-12
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Berotralstat Dihydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HETERO LABS LIMITED
Marketing Category
BULK INGREDIENT
Substance
BEROTRALSTAT DIHYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2020-12-03
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Ivacaftor
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HETERO LABS LIMITED
Marketing Category
BULK INGREDIENT
Substance
IVACAFTOR
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2012-01-31
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Apalutamide Premix
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HETERO LABS LIMITED
Marketing Category
BULK INGREDIENT
Substance
APALUTAMIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2018-02-14
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Crizotinib
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HETERO LABS LIMITED
Marketing Category
BULK INGREDIENT
Substance
CRIZOTINIB
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2011-08-26
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Sotorasib
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
SOTORASIB
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2021-05-28
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Belumosudil Mesylate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HETERO LABS LIMITED
Marketing Category
BULK INGREDIENT
Substance
BELUMOSUDIL MESYLATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2021-07-16
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Abemaciclib
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HETERO LABS LIMITED
Marketing Category
BULK INGREDIENT
Substance
ABEMACICLIB
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-09-28
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Opicapone
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HETERO LABS LIMITED
Marketing Category
BULK INGREDIENT
Substance
OPICAPONE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2020-04-24
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Avacopan
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HETERO LABS LIMITED
Marketing Category
BULK INGREDIENT
Substance
AVACOPAN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2021-10-07
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Lenacapavir Spray-Dried Dispersion
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HETERO LABS LIMITED
Marketing Category
BULK INGREDIENT
Substance
LENACAPAVIR SODIUM
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2022-12-22
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Dasatinib
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HETERO LABS LIMITED
Marketing Category
BULK INGREDIENT
Substance
DASATINIB
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2006-06-28
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Vismodegib
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HETERO LABS LIMITED
Marketing Category
BULK INGREDIENT
Substance
VISMODEGIB
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2012-01-30
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Belzutifan Premix
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HETERO LABS LIMITED
Marketing Category
BULK INGREDIENT
Substance
BELZUTIFAN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2021-08-13
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Ezetimibe (Form-B)
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HETERO LABS LIMITED
Marketing Category
BULK INGREDIENT
Substance
EZETIMIBE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2025-05-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Asciminib Hydrochloride Premix
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hetero Labs Limited
Marketing Category
BULK INGREDIENT
Substance
ASCIMINIB HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2021-10-29
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Lenacapavir
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HETERO LABS LIMITED
Marketing Category
BULK INGREDIENT
Substance
LENACAPAVIR SODIUM
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2022-12-22
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
RIMEGEPANT HEMISULFATE SESQUIHYDRATE
Dosage Form
POWDER
Strength
10 kg/10kg
Labeler
HETERO LABS LIMITED
Marketing Category
BULK INGREDIENT
Substance
RIMEGEPANT
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2020-02-27
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Zanubrutinib
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HETERO LABS LIMITED
Marketing Category
BULK INGREDIENT
Substance
ZANUBRUTINIB
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2025-06-10
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Ponatinib Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HETERO LABS LIMITED
Marketing Category
BULK INGREDIENT
Substance
PONATINIB HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2012-12-14
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Vericiguat
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HETERO LABS LIMITED
Marketing Category
BULK INGREDIENT
Substance
VERICIGUAT
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2021-01-19
End Marketing Date
-
Listing Record Certified Through
2027-12-31
NDC Type Breakdown
162 total- Bulk Ingredient
Official Source
NDC data is based on publicly available National Drug Code information from the U.S. Food and Drug Administration (FDA).
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NDC
68554-0001
Nonproprietary Name
Bicalutamide (Form-H1)
Labeler
Hetero Labs Limited
Dosage Form
POWDER
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