Zhejiang Supor Pharmaceuticals Co., LTD
NDC Database
Zhejiang Supor Pharmaceuticals Co., LTD
NDC Database
National Drug Code (NDC) records including drug products, NDC numbers, nonproprietary names, dosage forms, strengths, labelers and marketing information.
- Total Records 14
- Latest Marketing Date 2025-11-27
- Data Source FDA
- First Marketing Date 2010-08-16
Company Overview
Company
Zhejiang Supor Pharmaceuticals Co., LTD
Country
China
Website
Social Profiles
Company Snapshot
Zhejiang Supor Pharmaceuticals Co., LTD
Yuedong Road, Paojiang Industrial Zone, Shaoxing, Zhejiang, 312071, China
China
www.suporpharm.com/ suporpharm@suporpharm.com View on MapNDC Records ( 14 records )
Nonproprietary Name
Bupropion Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Zhejiang Supor Pharmaceuticals Co., Ltd
Marketing Category
BULK INGREDIENT
Substance
BUPROPION HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2010-09-15
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Quetiapine Fumarate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Zhejiang Supor Pharmaceuticals Co., Ltd
Marketing Category
BULK INGREDIENT
Substance
QUETIAPINE FUMARATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2010-09-13
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Tinidazole
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Zhejiang Supor Pharmaceuticals Co., Ltd
Marketing Category
BULK INGREDIENT
Substance
TINIDAZOLE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2010-08-16
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Felodipine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Zhejiang Supor Pharmaceuticals Co., Ltd
Marketing Category
BULK INGREDIENT
Substance
FELODIPINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2010-08-16
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Secnidazole
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Zhejiang Supor Pharmaceuticals Co., Ltd
Marketing Category
BULK INGREDIENT
Substance
SECNIDAZOLE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2010-08-16
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Olanzapine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Zhejiang Supor Pharmaceuticals Co., Ltd
Marketing Category
BULK INGREDIENT
Substance
OLANZAPINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2010-08-16
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Lamotrigine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Zhejiang Supor Pharmaceuticals Co., Ltd
Marketing Category
BULK INGREDIENT
Substance
LAMOTRIGINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2010-08-16
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Ornidazole
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Zhejiang Supor Pharmaceuticals Co., Ltd
Marketing Category
BULK INGREDIENT
Substance
ORNIDAZOLE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2010-08-16
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Ketotifen Fumarate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Zhejiang Supor Pharmaceuticals Co., Ltd
Marketing Category
BULK INGREDIENT
Substance
KETOTIFEN FUMARATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2012-10-31
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Rivaroxaban
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Zhejiang Supor Pharmaceuticals Co., Ltd
Marketing Category
BULK INGREDIENT
Substance
RIVAROXABAN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2014-12-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Vasopressin
Dosage Form
POWDER
Strength
1 g/g
Labeler
Zhejiang Supor Pharmaceuticals Co., Ltd
Marketing Category
BULK INGREDIENT
Substance
VASOPRESSIN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2014-04-17
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Degarelix Acetate
Dosage Form
POWDER
Strength
1 g/g
Labeler
Zhejiang Supor Pharmaceuticals Co., Ltd
Marketing Category
BULK INGREDIENT
Substance
ARGIPRESSIN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2022-06-15
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Leuprolide Acetate
Dosage Form
POWDER
Strength
1 g/g
Labeler
Zhejiang Supor Pharmaceuticals Co., Ltd
Marketing Category
BULK INGREDIENT
Substance
LEUPROLIDE ACETATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2024-10-31
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Degarelix Acetate
Dosage Form
POWDER
Strength
1 g/g
Labeler
Zhejiang Supor Pharmaceuticals Co., Ltd
Marketing Category
BULK INGREDIENT
Substance
DEGARELIX ACETATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2025-11-27
End Marketing Date
-
Listing Record Certified Through
2026-12-31
NDC Type Breakdown
14 total- Bulk Ingredient
Official Source
NDC data is based on publicly available National Drug Code information from the U.S. Food and Drug Administration (FDA).
Visit FDA NDC DirectoryNDC Record Details Preview
Explore important National Drug Code information available in the records above.
NDC
14799-0213
Nonproprietary Name
Bupropion Hydrochloride
Labeler
Zhejiang Supor Pharmaceuticals Co., Ltd
Dosage Form
POWDER
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