National Drug Code (NDC) Database
R. Mason (Chemicals) Ltd
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NDC:
46582-0002
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Nonproprietary Name:
Selenium Disulfide
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
SELENIUM SULFIDE
-
Start Marketing Date:
2010-03-11
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
R.L.Fine Chem Private Limited
-
NDC:
71554-124
-
Nonproprietary Name:
Calcium Gluconate
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
CALCIUM GLUCONATE
-
Start Marketing Date:
2026-05-13
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Ragolds USA Inc.
-
NDC:
84437-001
-
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:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Raks Pharma Pvt. Limited
-
NDC:
47621-313
-
Nonproprietary Name:
Metaxalone
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
METAXALONE
-
Start Marketing Date:
2026-03-27
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
RAKSHIT DRUGS PRIVATE LIMITED
-
NDC:
82139-0028
-
Nonproprietary Name:
Leflunomide
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
LEFLUNOMIDE
-
Start Marketing Date:
2025-11-14
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
RB Health (US) LLC
-
NDC:
72854-232
-
Nonproprietary Name:
Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride, and Triprolidine Hydrochloride
-
Dosage Form:
TABLET, COATED
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
325; 10; 5; 1.25 mg/1; mg/1; mg/1; mg/1
-
Substance:
ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE; TRIPROLIDINE HYDROCHLORIDE
-
Start Marketing Date:
2021-06-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Recipharm pharmaservices Private Limited
-
NDC:
51128-307
-
Nonproprietary Name:
Acetaminophen and Ibuprofen Tablets
-
Dosage Form:
TABLET
-
Product Type:
HUMAN PRESCRIPTION DRUG
-
Strength:
250; 125 mg/1; mg/1
-
Substance:
ACETAMINOPHEN; IBUPROFEN
-
Start Marketing Date:
2023-08-24
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Regeneron Pharmaceuticals, Inc
-
NDC:
61755-930
-
Nonproprietary Name:
aflibercept
-
Dosage Form:
INJECTION, SOLUTION
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
50 mg/mL
-
Substance:
AFLIBERCEPT
-
Start Marketing Date:
2012-08-03
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Regeneron Pharmaceuticals, Inc.
-
NDC:
61755-965
-
Nonproprietary Name:
odesivimab
-
Dosage Form:
INJECTION, SOLUTION
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
100 mg/mL
-
Substance:
ODESIVIMAB
-
Start Marketing Date:
2021-07-29
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
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