National Drug Code (NDC) Database
NuCare Pharmaceuticals,Inc.
-
NDC:
70859-102
-
Nonproprietary Name:
Methylene Blue
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 g/g
-
Substance:
METHYLENE BLUE
-
Start Marketing Date:
2026-03-20
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Nutriplant Industria Comercio S.A.
-
NDC:
82807-003
-
Nonproprietary Name:
Sodium Monofluorophosphate
-
Dosage Form:
POWDER, FOR SOLUTION
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
SODIUM MONOFLUOROPHOSPHATE
-
Start Marketing Date:
2023-03-20
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Nutriplant Industria e Comércio S.A.
-
NDC:
82807-002
-
Nonproprietary Name:
Sodium Fluoride
-
Dosage Form:
POWDER, FOR SOLUTION
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
SODIUM FLUORIDE
-
Start Marketing Date:
2007-01-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
OCB Pharmaceutical S.R.L.
-
NDC:
54474-0007
-
Nonproprietary Name:
Bismuth Hydroxide
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
BISMUTH HYDROXIDE
-
Start Marketing Date:
2014-02-12
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
oleon
-
NDC:
73031-001
-
Nonproprietary Name:
glycerin
-
Dosage Form:
LIQUID
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
GLYCERIN
-
Start Marketing Date:
2019-09-27
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
OLON ACTIVE PHARMACEUTICAL INGREDIENTS INDIA PRIVATE LIMITED
-
NDC:
73005-0011
-
Nonproprietary Name:
Lansoprazole
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
LANSOPRAZOLE
-
Start Marketing Date:
2024-02-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Olon Ricerca Bioscience, LLC
-
NDC:
71604-0001
-
Nonproprietary Name:
Rotigotine Polymorph II
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
ROTIGOTINE
-
Start Marketing Date:
2017-08-03
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Olon S.p.A.
-
NDC:
17337-0559
-
Nonproprietary Name:
Amiloride Hydrochloride
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
AMILORIDE HYDROCHLORIDE
-
Start Marketing Date:
2025-07-23
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
58159-134
-
Nonproprietary Name:
Benzgalantamine Gluconate
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
35 kg/35kg
-
Substance:
GALANTAMINE
-
Start Marketing Date:
2026-05-22
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
-
NDC:
51660-939
-
Nonproprietary Name:
Cetirizine Hydrochloride
-
Dosage Form:
TABLET
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
10 mg/1
-
Substance:
CETIRIZINE HYDROCHLORIDE
-
Start Marketing Date:
2024-11-28
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
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