National Drug Code (NDC) Database
Wuhan Calmland Pharmaceuticals Co., Ltd.
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NDC:
70747-1007
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Nonproprietary Name:
Methotrexate Disodium
-
Dosage Form:
INJECTION
-
Product Type:
BULK INGREDIENT
-
Strength:
25 mg/25mg
-
Substance:
METHOTREXATE SODIUM
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Start Marketing Date:
2026-05-29
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Wuhan Wuyao Pharmaceutical Co., Ltd.
-
NDC:
65832-0007
-
Nonproprietary Name:
Epinephrine
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
EPINEPHRINE
-
Start Marketing Date:
2010-06-11
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
WuXi Biologics Co., Ltd
-
NDC:
71851-005
-
Nonproprietary Name:
pemivibart
-
Dosage Form:
INJECTION
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
125 mg/mL
-
Substance:
PEMIVIBART
-
Start Marketing Date:
2024-03-22
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Wuxi Biologics Co., Ltd.
-
NDC:
71851-008
-
Nonproprietary Name:
denosumab-bnht
-
Dosage Form:
INJECTION
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
120 mg/1.7mL
-
Substance:
DENOSUMAB
-
Start Marketing Date:
2025-03-25
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
65050-0527
-
Nonproprietary Name:
Cantharidin
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 g/g
-
Substance:
CANTHARIDIN
-
Start Marketing Date:
2022-03-10
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Wuxi Fortune Pharmaceutical Co.,Ltd.
-
NDC:
65050-2101
-
Nonproprietary Name:
Mycophenolate Mofetil
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
MYCOPHENOLATE MOFETIL
-
Start Marketing Date:
2021-01-05
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Wuzhou Huangpu Chemical Pharmaceutical Co., Ltd.
-
NDC:
58811-7622
-
Nonproprietary Name:
CAMPHOR (SYNTHETIC)
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
CAMPHOR (SYNTHETIC)
-
Start Marketing Date:
2010-07-28
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Wyeth BioPharma Division of Wyeth Pharmaceuticals LLC
-
NDC:
58394-095
-
Nonproprietary Name:
bevacizumab
-
Dosage Form:
LIQUID
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
95.5 mg/95.5mL
-
Substance:
BEVACIZUMAB
-
Start Marketing Date:
2019-09-19
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Xellia (Taizhou) Pharmaceuticals Co., Ltd
-
NDC:
44231-0005
-
Nonproprietary Name:
Bacitracin
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
BACITRACIN
-
Start Marketing Date:
2012-12-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Xellia (Taizhou) Pharmaceuticals Co., Ltd.
-
NDC:
44231-0003
-
Nonproprietary Name:
Bacitracin Zinc
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
BACITRACIN ZINC
-
Start Marketing Date:
2012-12-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
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