Natco Pharma
NDC Database
Natco Pharma
NDC Database
National Drug Code (NDC) records including drug products, NDC numbers, nonproprietary names, dosage forms, strengths, labelers and marketing information.
- Total Records 45
- Latest Marketing Date 2026-05-16
- Data Source FDA
- First Marketing Date 2005-11-23
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Company Snapshot
NDC Records ( 45 records )
Nonproprietary Name
Ondansetron
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Natco Pharma Limited
Marketing Category
BULK INGREDIENT
Substance
ONDANSETRON HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2016-01-12
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
LANTHANUM CARBONATE DIHYDRATE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Natco Pharma Limited
Marketing Category
BULK INGREDIENT
Substance
LANTHANUM CARBONATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2005-11-23
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
OMEPRAZOLE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Natco Pharma Limited
Marketing Category
BULK INGREDIENT
Substance
OMEPRAZOLE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2016-01-21
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
PANTOPRAZOLE SODIUM
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Natco Pharma Limited
Marketing Category
BULK INGREDIENT
Substance
PANTOPRAZOLE SODIUM
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2016-01-21
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
LANSOPRAZOLE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Natco Pharma Limited
Marketing Category
BULK INGREDIENT
Substance
LANSOPRAZOLE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2016-01-21
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
citalopram
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Natco Pharma Limited
Marketing Category
BULK INGREDIENT
Substance
CITALOPRAM HYDROBROMIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2016-01-12
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Salmeterol
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Natco Pharma Limited
Marketing Category
BULK INGREDIENT
Substance
SALMETEROL XINAFOATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2016-01-20
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Glatiramer Acetate
Dosage Form
INJECTION
Strength
1 kg/kg
Labeler
Natco Pharma Limited
Marketing Category
BULK INGREDIENT
Substance
GLATIRAMER ACETATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-12-09
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
ZOLMITRIPTAN
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Natco Pharma Limited
Marketing Category
BULK INGREDIENT
Substance
ZOLMITRIPTAN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2016-01-21
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Ibandronate Sodium
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Natco Pharma Limited
Marketing Category
BULK INGREDIENT
Substance
IBANDRONATE SODIUM
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2016-01-12
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Imatinib
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Natco Pharma Limited
Marketing Category
BULK INGREDIENT
Substance
IMATINIB MESYLATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2016-01-20
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
ANASTROZOLE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Natco Pharma Limited
Marketing Category
BULK INGREDIENT
Substance
ANASTROZOLE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2016-01-21
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
TRIHEXYPHENIDYL
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Natco Pharma Limited
Marketing Category
BULK INGREDIENT
Substance
TRIHEXYPHENIDYL HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2016-01-21
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Zoledronic Acid
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Natco Pharma Limited
Marketing Category
BULK INGREDIENT
Substance
ZOLEDRONIC ACID
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2016-01-20
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Rizatriptan
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Natco Pharma Limited
Marketing Category
BULK INGREDIENT
Substance
RIZATRIPTAN BENZOATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2016-01-18
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Rizatriptan
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Natco Pharma Limited
Marketing Category
BULK INGREDIENT
Substance
RIZATRIPTAN BENZOATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2016-01-18
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Granisetron
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Natco Pharma Limited
Marketing Category
BULK INGREDIENT
Substance
GRANISETRON HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2016-01-12
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Lapatinib Ditosylate Anhydrous
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Natco Pharma Limited
Marketing Category
BULK INGREDIENT
Substance
LAPATINIB DITOSYLATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2021-05-17
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Erlotinib
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Natco Pharma Limited
Marketing Category
BULK INGREDIENT
Substance
ERLOTINIB HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2016-01-21
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Letrozole
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Natco Pharma Limited
Marketing Category
BULK INGREDIENT
Substance
LETROZOLE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2016-01-12
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Letrozole
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Natco Pharma Limited
Marketing Category
BULK INGREDIENT
Substance
LETROZOLE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2016-01-19
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Sorafenib
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Natco Pharma Limited
Marketing Category
BULK INGREDIENT
Substance
SORAFENIB TOSYLATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2016-01-20
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
GEFITINIB
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Natco Pharma Limited
Marketing Category
BULK INGREDIENT
Substance
GEFITINIB
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2020-01-04
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Chloroquine Phosphate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Natco Pharma Limited
Marketing Category
BULK INGREDIENT
Substance
CHLOROQUINE PHOSPHATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2018-03-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Teriflunomide
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Natco Pharma Limited
Marketing Category
BULK INGREDIENT
Substance
TERIFLUNOMIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-12-09
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
APIXABAN
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Natco Pharma Limited
Marketing Category
BULK INGREDIENT
Substance
APIXABAN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-09-12
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
IBRUTINIB
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Natco Pharma Limited
Marketing Category
BULK INGREDIENT
Substance
IBRUTINIB
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2020-01-04
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Idelalisib
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Natco Pharma Limited
Marketing Category
BULK INGREDIENT
Substance
IDELALISIB
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2023-11-25
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Sugammadex Sodium
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Natco Pharma Limited
Marketing Category
BULK INGREDIENT
Substance
SUGAMMADEX SODIUM
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2019-01-30
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Venetoclax
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Natco Pharma Limited
Marketing Category
BULK INGREDIENT
Substance
VENETOCLAX
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2023-11-29
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
nILOTINIB HYDROCHLORIDE MONOHYDRATE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Natco Pharma Limited
Marketing Category
BULK INGREDIENT
Substance
NILOTINIB HYDROCHLORIDE MONOHYDRATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2021-05-19
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Acalabrutinib Dihydrate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Natco Pharma Limited
Marketing Category
BULK INGREDIENT
Substance
ACALABRUTINIB DIHYDRATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2023-11-25
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Ruxolitinib Phosphate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Natco Pharma Limited
Marketing Category
BULK INGREDIENT
Substance
RUXOLITINIB PHOSPHATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2023-11-24
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Imatinib
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Natco Pharma Limited
Marketing Category
BULK INGREDIENT
Substance
IMATINIB MESYLATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2026-05-16
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
bendamustine hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
NATCO PHARMA LIMITED
Marketing Category
BULK INGREDIENT
Substance
BENDAMUSTINE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2015-11-19
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Bortezomib
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
NATCO PHARMA LIMITED
Marketing Category
BULK INGREDIENT
Substance
BORTEZOMIB
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2015-11-19
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
EVEROLIMUS
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
NATCO PHARMA LIMITED
Marketing Category
BULK INGREDIENT
Substance
EVEROLIMUS
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2015-11-19
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Thiotepa
Dosage Form
POWDER
Strength
0.1 kg/.1kg
Labeler
NATCO PHARMA LIMITED
Marketing Category
BULK INGREDIENT
Substance
THIOTEPA
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-12-09
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Pomalidomide
Dosage Form
POWDER
Strength
0.1 kg/.1kg
Labeler
NATCO PHARMA LIMITED
Marketing Category
BULK INGREDIENT
Substance
POMALIDOMIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-12-09
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Carmustine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
NATCO PHARMA LIMITED
Marketing Category
BULK INGREDIENT
Substance
CARMUSTINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2020-02-19
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Trifluridine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
NATCO PHARMA LIMITED
Marketing Category
BULK INGREDIENT
Substance
TRIFLURIDINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2018-05-02
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Tipiracil Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
NATCO PHARMA LIMITED
Marketing Category
BULK INGREDIENT
Substance
TIPIRACIL HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2018-12-19
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
TRABECTEDIN
Dosage Form
INJECTION
Strength
1 g/g
Labeler
NATCO PHARMA LIMITED
Marketing Category
BULK INGREDIENT
Substance
TRABECTEDIN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2021-08-25
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Cidofovir Dihydrate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
NATCO PHARMA LIMITED
Marketing Category
BULK INGREDIENT
Substance
CIDOFOVIR
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2023-11-27
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Erdafitinib
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
NATCO PHARMA LIMITED
Marketing Category
BULK INGREDIENT
Substance
ERDAFITINIB
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2023-11-28
End Marketing Date
-
Listing Record Certified Through
2026-12-31
NDC Type Breakdown
45 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
63850-2706
Nonproprietary Name
Ondansetron
Labeler
Natco Pharma Limited
Dosage Form
POWDER
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