National Drug Code (NDC) Database
-
NDC:
65415-1372
-
Nonproprietary Name:
Nystatin
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
NYSTATIN
-
Start Marketing Date:
2014-03-20
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Anthem Biosciences Limited
-
NDC:
76438-007
-
Nonproprietary Name:
PALTUSOTINE HYDROCHLORIDE
-
Dosage Form:
POWDER
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
1 mg/mg
-
Substance:
PALTUSOTINE HYDROCHLORIDE
-
Start Marketing Date:
2026-04-30
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Antibioticos do Brasil Ltda.
-
NDC:
10402-021
-
Nonproprietary Name:
Cephalothin Sodium
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
CEPHALOTHIN SODIUM
-
Start Marketing Date:
2011-06-28
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
ANUH PHARMA LIMITED
-
NDC:
64677-0011
-
Nonproprietary Name:
CHLORAMPHENICOL PALMITATE
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
CHLORAMPHENICOL PALMITATE
-
Start Marketing Date:
2025-12-31
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Anuh Pharma Ltd.
-
NDC:
64677-0001
-
Nonproprietary Name:
ERYTHROMYCIN ETHYL SUCCINATE
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
ERYTHROMYCIN ETHYLSUCCINATE
-
Start Marketing Date:
2019-04-22
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Aperture Pharmaceuticals LLC
-
NDC:
85699-010
-
Nonproprietary Name:
Pentobarbital Sodium
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
250 g/250g
-
Substance:
PENTOBARBITAL SODIUM
-
Start Marketing Date:
2025-08-13
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
CII
-
Certified Through:
2026-12-31
Apicore Pharmaceuticals Private Limited
-
NDC:
42973-434
-
Nonproprietary Name:
Ferric carboxymaltose
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
FERRIC CARBOXYMALTOSE
-
Start Marketing Date:
2026-03-14
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
-
NDC:
10402-013
-
Nonproprietary Name:
CEFTAZIDIME
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 g/g
-
Substance:
CEFTAZIDIME
-
Start Marketing Date:
2010-01-20
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
69617-016
-
Nonproprietary Name:
Meloxicam
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
25 kg/25kg
-
Substance:
MELOXICAM
-
Start Marketing Date:
2025-11-13
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
81666-010
-
Nonproprietary Name:
Xanomeline Tartrate
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
XANOMELINE TARTRATE
-
Start Marketing Date:
2025-11-29
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
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