National Drug Code (NDC) Database
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NDC:
66122-0009
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Nonproprietary Name:
AZATHIOPRINE
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
AZATHIOPRINE
-
Start Marketing Date:
2019-12-13
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Zhejiang Cheng Yi Pharmaceutical Co., Ltd.
-
NDC:
66122-0016
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Nonproprietary Name:
MERCAPTOPURINE MONOHYDRATE
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
MERCAPTOPURINE
-
Start Marketing Date:
2019-12-13
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Zhejiang Chiral Medicine Chemicals Co., Ltd.
-
NDC:
67628-3001
-
Nonproprietary Name:
METHYLDOPA
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
METHYLDOPA
-
Start Marketing Date:
2013-08-09
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Zhejiang Dayang Biotech Group Co. Ltd.
-
NDC:
53841-0001
-
Nonproprietary Name:
AMPROLIUM
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
AMPROLIUM
-
Start Marketing Date:
2013-04-09
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
ZHEJIANG ESIGMA BIOTECHNOLOGY CO., LTD.
-
NDC:
87787-401
-
Nonproprietary Name:
Decoquinate
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
DECOQUINATE
-
Start Marketing Date:
2026-06-22
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Zhejiang Excel Pharmaceutical Co., Ltd.
-
NDC:
15440-1025
-
Nonproprietary Name:
Gemfibrozil
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
GEMFIBROZIL
-
Start Marketing Date:
2006-09-14
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
51943-130
-
Nonproprietary Name:
CLARITHROMYCIN
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
CLARITHROMYCIN
-
Start Marketing Date:
2023-08-18
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
69984-001
-
Nonproprietary Name:
Sucralfate
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
SUCRALFATE
-
Start Marketing Date:
2016-01-19
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Zhejiang Haizhou Pharmaceutical Co., Ltd.
-
NDC:
65072-0801
-
Nonproprietary Name:
Iohexol
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
IOHEXOL
-
Start Marketing Date:
2020-07-10
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
67321-568
-
Nonproprietary Name:
FLORFENICOL
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
FLORFENICOL
-
Start Marketing Date:
2015-02-22
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
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