National Drug Code (NDC) Database
Cadila Pharmaceuticals Limited
-
NDC:
65691-0128
-
Nonproprietary Name:
Rivaroxaban
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
25 kg/25kg
-
Substance:
RIVAROXABAN
-
Start Marketing Date:
2026-05-13
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Calyx Chemcials & Pharmaceuticals
-
NDC:
66639-003
-
Nonproprietary Name:
Erythromycin Stearate
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
ERYTHROMYCIN STEARATE
-
Start Marketing Date:
2009-09-02
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Calyx Chemicals & Pharmaceuticals
-
NDC:
66639-023
-
Nonproprietary Name:
Azaerythromycin
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
AZAERYTHROMYCIN A
-
Start Marketing Date:
2019-01-18
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Camber Consumer Care Inc
-
NDC:
69230-327
-
Nonproprietary Name:
famotidine
-
Dosage Form:
TABLET, FILM COATED
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
20 mg/1
-
Substance:
FAMOTIDINE
-
Start Marketing Date:
2021-11-08
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Cambrex Profarmaco Milano S.r.l.
-
NDC:
12828-0089
-
Nonproprietary Name:
RIFAXIMIN
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
RIFAXIMIN
-
Start Marketing Date:
2016-11-09
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Cambridge Isotope Laboratories, Inc.
-
NDC:
61444-901
-
Nonproprietary Name:
UREA C-13
-
Dosage Form:
POWDER, FOR SOLUTION
-
Product Type:
BULK INGREDIENT
-
Strength:
1 g/g
-
Substance:
UREA C-13
-
Start Marketing Date:
1996-02-08
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Canada Packers Inc.
-
NDC:
70535-300
-
Nonproprietary Name:
crude heparin
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
HEPARIN SODIUM
-
Start Marketing Date:
2016-03-18
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
66639-914
-
Nonproprietary Name:
ISONIAZID
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
ISONIAZID
-
Start Marketing Date:
2009-09-24
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
59116-7560
-
Nonproprietary Name:
Methylphenidate Hydrochloride
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
METHYLPHENIDATE HYDROCHLORIDE
-
Start Marketing Date:
2013-08-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
CII
-
Certified Through:
2026-12-31
-
NDC:
58567-111
-
Nonproprietary Name:
Migalastat hydrochloride
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
MIGALASTAT HYDROCHLORIDE
-
Start Marketing Date:
2024-03-18
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
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