National Drug Code (NDC) Database
Sofgen Pharmaceuticals LLC
-
NDC:
70968-724
-
Nonproprietary Name:
IBUPROFEN
-
Dosage Form:
CAPSULE, LIQUID FILLED
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
200 mg/1
-
Substance:
IBUPROFEN
-
Start Marketing Date:
2025-08-27
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
SOLARA ACIVE PHARMA SCIENCES LIMITED
-
NDC:
72643-035
-
Nonproprietary Name:
MEBENDAZOLE
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
MEBENDAZOLE
-
Start Marketing Date:
2023-06-30
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Solara Active Pharma Sciences Limited
-
NDC:
72643-042
-
Nonproprietary Name:
Dexibuprofen
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
DEXIBUPROFEN
-
Start Marketing Date:
2025-01-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Solesence, Inc.
-
NDC:
63931-4489
-
Nonproprietary Name:
Zinc Oxide
-
Dosage Form:
SUSPENSION
-
Product Type:
BULK INGREDIENT
-
Strength:
1 g/g
-
Substance:
ZINC OXIDE
-
Start Marketing Date:
2022-07-21
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
55579-939
-
Nonproprietary Name:
LIDOCAINE HYDROCHLORIDE
-
Dosage Form:
LIQUID
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
10 mg/mL
-
Substance:
LIDOCAINE HYDROCHLORIDE ANHYDROUS
-
Start Marketing Date:
2018-08-03
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Solvay USA Inc.
-
NDC:
71834-001
-
Nonproprietary Name:
Nonoxynol 9
-
Dosage Form:
LIQUID
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
NONOXYNOL-9
-
Start Marketing Date:
2001-01-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Solventum US LLC
-
NDC:
17518-587
-
Nonproprietary Name:
Flurandrenolide
-
Dosage Form:
TAPE
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
4 ug/cm2
-
Substance:
FLURANDRENOLIDE
-
Start Marketing Date:
2016-08-15
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Sonneborn, LLC
-
NDC:
15592-7411
-
Nonproprietary Name:
White Petrolatum
-
Dosage Form:
OINTMENT
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
WHITE PETROLATUM
-
Start Marketing Date:
2022-03-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
54660-004
-
Nonproprietary Name:
OLIVE
-
Dosage Form:
OIL
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
OLIVE OIL
-
Start Marketing Date:
2022-01-03
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
70298-0260
-
Nonproprietary Name:
Methylprednisolone acetate
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
METHYLPREDNISOLONE ACETATE
-
Start Marketing Date:
2019-10-02
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
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