National Drug Code (NDC) Database
V. Mane Fils
-
NDC:
72702-002
-
Nonproprietary Name:
Thymol
-
Dosage Form:
CRYSTAL
-
Product Type:
BULK INGREDIENT
-
Strength:
225 kg/225kg
-
Substance:
THYMOL
-
Start Marketing Date:
2019-09-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
VALARY LAB LIMITED
-
NDC:
81955-0011
-
Nonproprietary Name:
Bendamustine Hydrochloride
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
BENDAMUSTINE HYDROCHLORIDE
-
Start Marketing Date:
2008-03-20
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
VALARY LAB PRIVATE LIMITED
-
NDC:
81955-0029
-
Nonproprietary Name:
DABRAFENIB MESYLATE
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
DABRAFENIB MESYLATE
-
Start Marketing Date:
2023-03-16
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
VALENS MOLECULES PRIVATE LIMITED
-
NDC:
62705-0230
-
Nonproprietary Name:
SULFADIAZINE
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
SULFADIAZINE
-
Start Marketing Date:
2023-04-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
VALENS PHARMACHEM PRIVATE LIMITED
-
NDC:
87070-001
-
Nonproprietary Name:
Cholestyramine Resin
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
100 g/100g
-
Substance:
CHOLESTYRAMINE
-
Start Marketing Date:
2025-09-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
VAMSI LABS LIMITED.
-
NDC:
66412-0771
-
Nonproprietary Name:
Haloperidol Decanoate
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 g/g
-
Substance:
HALOPERIDOL DECANOATE
-
Start Marketing Date:
2026-05-11
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Vannsh Life Sciences Private Limited
-
NDC:
87072-0002
-
Nonproprietary Name:
Carmustine
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
CARMUSTINE
-
Start Marketing Date:
2025-09-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
62147-0400
-
Nonproprietary Name:
glipizide
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
GLIPIZIDE
-
Start Marketing Date:
2009-08-05
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
83772-1001
-
Nonproprietary Name:
Ammonium Lactate Solution
-
Dosage Form:
SOLUTION
-
Product Type:
BULK INGREDIENT
-
Strength:
60 kg/100kg
-
Substance:
AMMONIUM LACTATE
-
Start Marketing Date:
2023-11-08
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Create a New Buying Request
Fields marked with * are mandatory.