National Drug Code (NDC) Database
Farmhispania S.A.
-
NDC:
17404-1035
-
Nonproprietary Name:
Rocuronium Bromide
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
ROCURONIUM BROMIDE
-
Start Marketing Date:
2025-11-19
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Farmhispania, S.A.
-
NDC:
17404-1034
-
Nonproprietary Name:
Everolimus
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
EVEROLIMUS
-
Start Marketing Date:
2025-07-28
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
FARMSON PHARMACEUTICAL GUJARAT PRIVATE LIMITED
-
NDC:
55794-202
-
Nonproprietary Name:
Acetaminophen
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
ACETAMINOPHEN
-
Start Marketing Date:
2023-09-09
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
FDC Limited
-
NDC:
55545-0706
-
Nonproprietary Name:
Nepafenac
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
NEPAFENAC
-
Start Marketing Date:
2024-10-04
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Febuxostat
-
NDC:
70966-0041
-
Nonproprietary Name:
Febuxostat
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
FEBUXOSTAT
-
Start Marketing Date:
2019-07-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Fermic, s.a. de c.v.
-
NDC:
39390-0046
-
Nonproprietary Name:
Clavulanate Potassium
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
CLAVULANATE POTASSIUM
-
Start Marketing Date:
2024-02-12
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Fertin Pharma A/S
-
NDC:
63443-5081
-
Nonproprietary Name:
nicotine polacrilex
-
Dosage Form:
GUM, CHEWING
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
4 mg/1
-
Substance:
NICOTINE
-
Start Marketing Date:
2019-06-30
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Fidelio Healthcare Limburg GmbH
-
NDC:
87383-010
-
Nonproprietary Name:
OLANZAPINE
-
Dosage Form:
TABLET, FILM COATED
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
20 mg/1
-
Substance:
OLANZAPINE
-
Start Marketing Date:
2026-02-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
-
NDC:
12780-6690
-
Nonproprietary Name:
methotrexate sodium
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
METHOTREXATE SODIUM
-
Start Marketing Date:
2010-01-14
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
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