Divis Laboratories
NDC Database
Divis Laboratories
NDC Database
National Drug Code (NDC) records including drug products, NDC numbers, nonproprietary names, dosage forms, strengths, labelers and marketing information.
- Total Records 51
- Latest Marketing Date 2026-04-10
- Data Source FDA
- First Marketing Date 1997-10-03
Company Overview
Social Profiles
Company Snapshot
Divis Laboratories
Divis Laboratories LimitedDivi Towers, 7-1-77/E/1/303,Dharam Karan Road, Ameerpet,HYDERABAD - 500 016.Andhra Pradesh, India.
India
www.divislabs.com/ amitha@divislabs.com View on MapNDC Records ( 51 records )
Nonproprietary Name
Naproxen
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Divi's Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
NAPROXEN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1999-01-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Naproxen Sodium
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Divi's Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
NAPROXEN SODIUM
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1999-01-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Dextromethorphan Hydrobromide
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Divi's Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
DEXTROMETHORPHAN HYDROBROMIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2002-01-03
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Dextromethorphan Hydrobromide
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Divi's Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
DEXTROMETHORPHAN HYDROBROMIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2002-01-03
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Dextromethorphan
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Divi's Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
DEXTROMETHORPHAN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2002-02-13
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Diltiazem Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Divi's Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
DILTIAZEM HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1997-10-03
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Iopamidol
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Divi's Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
IOPAMIDOL
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2005-12-13
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Nabumetone
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Divi's Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
NABUMETONE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2000-01-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Nabumetone
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Divi's Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
NABUMETONE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2025-11-17
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Levetiracetam
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Divi's Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
LEVETIRACETAM
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2002-12-24
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Levodopa
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Divi's Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
LEVODOPA
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2004-03-17
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Carbidopa
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Divi's Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
CARBIDOPA
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2004-03-29
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Niacin
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Divi's Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
NIACIN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2004-07-20
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Desloratadine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Divi's Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
DESLORATADINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2004-11-11
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Proguanil Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Divi's Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
PROGUANIL HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2004-05-31
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Tamsulosin Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Divi's Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
TAMSULOSIN HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2004-04-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Bupropion Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Divi's Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
BUPROPION HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2006-08-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Phenylephrine Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Divi's Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
PHENYLEPHRINE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2002-01-04
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Naproxen
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Divi's Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
NAPROXEN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2006-08-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Naproxen Sodium
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Divi's Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
NAPROXEN SODIUM
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2006-08-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Gabapentin
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Divi's Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
GABAPENTIN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2005-09-07
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Valacyclovir Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Divi's Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
VALACYCLOVIR HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2026-04-10
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Valacyclovir Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Divi's Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
VALACYCLOVIR HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2006-03-28
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Carvedilol
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Divi's Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
CARVEDILOL
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2006-01-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Quetiapine Fumarate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Divi's Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
QUETIAPINE FUMARATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2006-08-10
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Vigabatrin
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Divi's Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
VIGABATRIN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2007-08-18
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Capecitabine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Divi's Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
CAPECITABINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2007-08-29
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Venlafaxine Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Divi's Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
VENLAFAXINE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2008-06-09
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Orlistat
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Divi's Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
ORLISTAT
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2008-04-23
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Triprolidine Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Divi's Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
TRIPROLIDINE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2003-08-23
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Lamotrigine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Divi's Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
LAMOTRIGINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2010-03-05
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Sumatriptan
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Divi's Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
SUMATRIPTAN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2009-06-24
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Sumatriptan Succinate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Divi's Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
SUMATRIPTAN SUCCINATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2009-04-02
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Valsartan
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Divi's Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
VALSARTAN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2010-01-28
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Irbesartan
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Divi's Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
IRBESARTAN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2010-03-29
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Alexidine Dihydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Divi's Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
ALEXIDINE DIHYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2010-08-31
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Raltegravir Potassium
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Divi's Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
RALTEGRAVIR POTASSIUM
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2008-05-28
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Olmesartan Medoxomil
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Divi's Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
OLMESARTAN MEDOXOMIL
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2012-11-21
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Pregabalin
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Divi's Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
PREGABALIN
Product Type
BULK INGREDIENT
DEA Schedule
CV
Start Marketing Date
2012-09-07
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Valacyclovir Hydrochloride (Hydrous form)
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Divi's Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
VALACYCLOVIR HYDROCHLORIDE MONOHYDRATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2014-11-14
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Atovaquone
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Divi's Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
ATOVAQUONE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2007-04-09
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Mesalamine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Divi's Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
MESALAMINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2015-03-02
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Lacosamide
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Divi's Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
LACOSAMIDE
Product Type
BULK INGREDIENT
DEA Schedule
CV
Start Marketing Date
2020-09-21
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Molnupiravir
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Divi's Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
MOLNUPIRAVIR
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2021-05-06
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Mesalamine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Divi's Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
MESALAMINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2022-09-19
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Mesalamine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Divi's Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
MESALAMINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2022-09-19
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Ticagrelor
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Divi's Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
TICAGRELOR
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2022-06-27
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Iohexol
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Divi's Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
IOHEXOL
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2022-07-04
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Foslevodopa
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Divi's Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
FOSLEVODOPA
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2025-06-24
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Foscarbidopa
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Divi's Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
FOSCARBIDOPA
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2025-06-24
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Xanomeline Tartrate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Divi's Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
XANOMELINE TARTRATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2026-04-09
End Marketing Date
-
Listing Record Certified Through
2027-12-31
NDC Type Breakdown
51 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
62331-001
Nonproprietary Name
Naproxen
Labeler
Divi's Laboratories Limited
Dosage Form
POWDER
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