National Drug Code (NDC) Database
Pharmacia Hepar LLC
-
NDC:
46655-1224
-
Nonproprietary Name:
Heparin Sodium
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
HEPARIN SODIUM
-
Start Marketing Date:
2014-07-03
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Pharmacosmos A/S
-
NDC:
49442-5800
-
Nonproprietary Name:
Dextran
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 g/g
-
Substance:
DEXTRAN 1
-
Start Marketing Date:
2015-06-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
PHARMAKINA S.A.
-
NDC:
67729-001
-
Nonproprietary Name:
QUININE SULFATE
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
QUININE SULFATE
-
Start Marketing Date:
1961-01-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Pharmaloz Manufacturing Inc
-
NDC:
61941-9502
-
Nonproprietary Name:
Menthol
-
Dosage Form:
LOZENGE
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
7 mg/1
-
Substance:
MENTHOL, UNSPECIFIED FORM
-
Start Marketing Date:
2004-11-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Pharmaloz Manufacturing Inc.
-
NDC:
61941-9302
-
Nonproprietary Name:
Menthol
-
Dosage Form:
LOZENGE
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
7 mg/1
-
Substance:
MENTHOL, UNSPECIFIED FORM
-
Start Marketing Date:
2004-11-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Pharmaron (Ningbo) Technology Development Co., Ltd.
-
NDC:
84783-101
-
Nonproprietary Name:
Etripamil
-
Dosage Form:
OIL
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
ETRIPAMIL, (R)-
-
Start Marketing Date:
2025-12-13
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Pharmaron Manufacturing Services (UK) Ltd
-
NDC:
61891-022
-
Nonproprietary Name:
Naloxone
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
100 g/100g
-
Substance:
NALOXONE HYDROCHLORIDE DIHYDRATE
-
Start Marketing Date:
2017-04-18
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Pharmatory Oy
-
NDC:
71362-003
-
Nonproprietary Name:
Atipamezole Hydrochloride
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
ATIPAMEZOLE HYDROCHLORIDE
-
Start Marketing Date:
2022-11-09
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
-
NDC:
60050-004
-
Nonproprietary Name:
Metoprolol Succinate
-
Dosage Form:
TABLET, EXTENDED RELEASE
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
200 mg/1
-
Substance:
METOPROLOL SUCCINATE
-
Start Marketing Date:
2020-12-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
12598-9643
-
Nonproprietary Name:
Chenodeoxycholic acid
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
CHENODIOL
-
Start Marketing Date:
2025-11-12
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
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