National Drug Code (NDC) Database
Sri Krishna Pharmaceutical Ltd. Unit I
-
NDC:
66326-505
-
Nonproprietary Name:
Folic Acid
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
FOLIC ACID
-
Start Marketing Date:
2019-12-23
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Sri Krishna Pharmaceuticals Limited
-
NDC:
66326-401
-
Nonproprietary Name:
Furosemide
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
FUROSEMIDE
-
Start Marketing Date:
2015-09-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Srikem Laboratories Pvt. Ltd.
-
NDC:
13746-120
-
Nonproprietary Name:
Umifenovir Hydrochloride Monohydrate
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
UMIFENOVIR HYDROCHLORIDE MONOHYDRATE
-
Start Marketing Date:
2021-11-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Srini Pharmaceuticals Private Limited
-
NDC:
66174-0091
-
Nonproprietary Name:
APIXABAN
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
APIXABAN
-
Start Marketing Date:
2021-11-23
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Srini Pharmaceuticals Private Limited.
-
NDC:
66174-0018
-
Nonproprietary Name:
LEVOFLOXACIN HEMIHYDRATE
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
LEVOFLOXACIN
-
Start Marketing Date:
2012-12-06
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
ST Pharm Co., Ltd.
-
NDC:
73675-008
-
Nonproprietary Name:
DONIDALORSEN SODIUM
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 g/g
-
Substance:
DONIDALORSEN SODIUM
-
Start Marketing Date:
2025-08-21
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
STELLA CHEMIFA CORPORATION
-
NDC:
58110-007
-
Nonproprietary Name:
Stannous Fluoride
-
Dosage Form:
CRYSTAL
-
Product Type:
BULK INGREDIENT
-
Strength:
100 kg/100kg
-
Substance:
STANNOUS FLUORIDE
-
Start Marketing Date:
2015-12-02
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Sterling Chemical Malta Ltd
-
NDC:
59057-019
-
Nonproprietary Name:
CABOZANTINIB
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
CABOZANTINIB
-
Start Marketing Date:
2024-09-02
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
66326-910
-
Nonproprietary Name:
Glipizide
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
GLIPIZIDE
-
Start Marketing Date:
2024-06-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
50384-6700
-
Nonproprietary Name:
Nilotinib Hydrochloride
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
350 kg/350kg
-
Substance:
NILOTINIB HYDROCHLORIDE MONOHYDRATE
-
Start Marketing Date:
2023-07-03
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Create a New Buying Request
Fields marked with * are mandatory.