National Drug Code (NDC) Database
-
NDC:
51040-000
-
Nonproprietary Name:
ALLANTOIN
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
ALLANTOIN
-
Start Marketing Date:
2012-06-07
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
ITM Medical Isotopes GmbH
-
NDC:
72665-003
-
Nonproprietary Name:
Lutetium (177Lu) chloride
-
Dosage Form:
SOLUTION
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
300 GBq/mL
-
Substance:
LUTETIUM CHLORIDE LU-177
-
Start Marketing Date:
2020-05-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
J P N PHARMA PRIVATE LIMITED
-
NDC:
50496-222
-
Nonproprietary Name:
Phenobarbital
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
PHENOBARBITAL
-
Start Marketing Date:
2025-03-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
CIV
-
Certified Through:
2026-12-31
J.M. Huber Micropowders, Inc.
-
NDC:
66218-901
-
Nonproprietary Name:
Calcium carbonate granulation with maltodextrin and mineral oil
-
Dosage Form:
GRANULE
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
475 kg/500kg
-
Substance:
CALCIUM CARBONATE
-
Start Marketing Date:
2021-04-02
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Jahnke Süsswaren GmbH
-
NDC:
71062-001
-
Nonproprietary Name:
menthol
-
Dosage Form:
LOZENGE
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
6 mg/1
-
Substance:
MENTHOL
-
Start Marketing Date:
2024-06-17
-
End Marketing Date:
2026-10-31
-
DEA Schedule:
-
Certified Through:
0000-00-00
Janssen Cilag SpA
-
NDC:
62579-726
-
Nonproprietary Name:
Cetirizine Hydrochloride
-
Dosage Form:
TABLET, FILM COATED
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
10 mg/1
-
Substance:
CETIRIZINE HYDROCHLORIDE
-
Start Marketing Date:
2008-10-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Janssen Pharamceutica NV
-
NDC:
12578-431
-
Nonproprietary Name:
Cisapride
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
CISAPRIDE
-
Start Marketing Date:
1999-08-10
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Janssen Pharmaceutica NV
-
NDC:
12578-890
-
Nonproprietary Name:
Galantamine hydrobromide
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
GALANTAMINE HYDROBROMIDE
-
Start Marketing Date:
2001-11-15
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Janssen Pharmaceutica, NV
-
NDC:
12578-622
-
Nonproprietary Name:
Rilpivirine
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
RILPIVIRINE
-
Start Marketing Date:
2021-01-21
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
17314-812
-
Nonproprietary Name:
darunavir ethanolate and cobicistat
-
Dosage Form:
TABLET, FILM COATED
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
150; 800 mg/1; mg/1
-
Substance:
COBICISTAT; DARUNAVIR ETHANOLATE
-
Start Marketing Date:
2015-01-31
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
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