National Drug Code (NDC) Database
Zhuhai Rundu Pharmaceutical Co., Ltd.
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NDC:
72023-0014
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Nonproprietary Name:
Valsartan
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Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
VALSARTAN
-
Start Marketing Date:
2024-12-26
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Zibo Xinhua - Perrigo Pharmaceutical Co., Ltd
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NDC:
16528-210
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Nonproprietary Name:
acetaminophen
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Dosage Form:
TABLET, FILM COATED
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
500 mg/1
-
Substance:
ACETAMINOPHEN
-
Start Marketing Date:
2021-09-29
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Zochem ULC
-
NDC:
46372-0000
-
Nonproprietary Name:
Zinc oxide
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
ZINC OXIDE
-
Start Marketing Date:
2015-05-28
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Zoetis Inc.
-
NDC:
54771-8451
-
Nonproprietary Name:
Nutritional Supplement
-
Dosage Form:
TABLET
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
0.04 mg/40mg
-
Substance:
POTASSIUM PHOSPHATE, UNSPECIFIED FORM
-
Start Marketing Date:
2024-12-17
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
ZUVCHEM
-
NDC:
87107-021
-
Nonproprietary Name:
CHOLECALCIFEROL
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
CHOLECALCIFEROL
-
Start Marketing Date:
2025-09-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Zydus Lifesciences Limited
-
NDC:
65841-302
-
Nonproprietary Name:
Phenylbutazone
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
PHENYLBUTAZONE
-
Start Marketing Date:
2025-09-27
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
¿Catalent Germany Eberbach GmbH
-
NDC:
55361-0033
-
Nonproprietary Name:
Talazoparib tosylate
-
Dosage Form:
CAPSULE
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
0.5 mg/1
-
Substance:
TALAZOPARIB TOSYLATE
-
Start Marketing Date:
2024-04-15
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
¿Pure Peptide Pharmaceuticals Inc.
-
NDC:
87551-090
-
Nonproprietary Name:
Epitalon Acetate
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 g/g
-
Substance:
EPITALON
-
Start Marketing Date:
2026-05-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
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