National Drug Code (NDC) Database
Jubilant Biosys limited
-
NDC:
65372-1206
-
Nonproprietary Name:
atorvastatin calcium amorphous
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
ATORVASTATIN CALCIUM ANHYDROUS
-
Start Marketing Date:
2008-08-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
59746-284
-
Nonproprietary Name:
Pantoprazole Sodium
-
Dosage Form:
TABLET, DELAYED RELEASE
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
40 mg/1
-
Substance:
PANTOPRAZOLE SODIUM
-
Start Marketing Date:
2011-09-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Jubilant HollisterStier LLC
-
NDC:
65044-7466
-
Nonproprietary Name:
collagenase clostridium histolyticum
-
Dosage Form:
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
0.9 mg/1
-
Substance:
COLLAGENASE CLOSTRIDIUM HISTOLYTICUM
-
Start Marketing Date:
2010-02-02
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Jubilant Pharmova Limited
-
NDC:
65372-1203
-
Nonproprietary Name:
vilazodone hydrochloride
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
VILAZODONE HYDROCHLORIDE
-
Start Marketing Date:
2019-07-26
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
JUSTESA IMAGEN S.A.U.
-
NDC:
52134-0500
-
Nonproprietary Name:
DIATRIZOIC ACID DIHYDRATE
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
DIATRIZOIC ACID
-
Start Marketing Date:
2009-08-11
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Justesa Imagen, S.A.U.
-
NDC:
52134-0503
-
Nonproprietary Name:
Iothalamic Acid
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
IOTHALAMIC ACID
-
Start Marketing Date:
2015-05-19
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
K+S Minerals and Agriculture GmbH
-
NDC:
70343-210
-
Nonproprietary Name:
Sodium chloride
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
SODIUM CHLORIDE
-
Start Marketing Date:
2017-08-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
-
NDC:
59361-005
-
Nonproprietary Name:
Lenvatinib Mesylate
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
LENVATINIB MESYLATE
-
Start Marketing Date:
2024-06-05
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
73276-002
-
Nonproprietary Name:
Calcium Sennosides
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
15 kg/15kg
-
Substance:
SENNOSIDES
-
Start Marketing Date:
2022-10-20
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
-
NDC:
69500-110
-
Nonproprietary Name:
SODIUM CHLORIDE
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
SODIUM CHLORIDE
-
Start Marketing Date:
2018-02-08
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
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