Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
01 1Granules India Limited
02 2Ofichem BV
03 1Aarti Pharmalabs Limited
04 1Alembic Pharmaceuticals Limited
05 1Aurobindo Pharma Limited
06 1Cadila Pharmaceuticals Limited
07 1Chemeca Drugs Private Limited
08 1Derivados Quimicos
09 3Dipharma Francis Srl
10 1Divi's Laboratories Limited
11 3Erregierre SpA
12 1Fagron Inc
13 1Glenmark Life Sciences Limited
14 1HIKAL LIMITED
15 1Hetero Drugs Limited
16 1Jubilant Pharmova Limited
17 1LETCO MEDICAL, LLC
18 1Medisca
19 1Olon S.p.A.
20 1Olon SpA
21 1Pharma Source Direct, Inc.
22 1Professional Compounding Centers of America
23 1Professional Compounding Centers of America dba PCCA
24 1Spectrum Chemicals and Laboratory Products
25 1Willow Birch Pharma, Inc
26 1Zhejiang Apeloa Jiayuan Pharmaceutical Co., Ltd.
27 1Zhejiang Supor Pharmaceuticals Co., Ltd
28 1Zydus Lifesciences Limited
01 1BUPROPION
02 6BUPROPION HYDROCHLORIDE
03 2Bupropion HCl
04 21Bupropion Hydrochloride
05 1R-Buproprion Hydrochloride
06 1S-Buproprion Hydrochloride
07 1bupropion hydrochloride
01 2China
02 12India
03 8Italy
04 3Netherlands
05 1Spain
06 5U.S.A
07 2United Kingdom
Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
NDC Package Code : 62207-976
Start Marketing Date : 2021-03-25
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Laboratorium Ofichem, offering a flexible, high-tech environment to produce broad range of APIs for Human & Vet pharmaceutical markets.
NDC Package Code : 62675-1456
Start Marketing Date : 2019-12-02
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
NDC Package Code : 15308-0412
Start Marketing Date : 2010-03-24
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Laboratorium Ofichem, offering a flexible, high-tech environment to produce broad range of APIs for Human & Vet pharmaceutical markets.
NDC Package Code : 62675-1524
Start Marketing Date : 2019-12-02
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 38779-3304
Start Marketing Date : 2024-02-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 17337-0012
Start Marketing Date : 2004-04-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 17337-0505
Start Marketing Date : 2020-03-03
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 10695-170
Start Marketing Date : 2024-08-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 12666-0001
Start Marketing Date : 2009-06-08
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 14799-0213
Start Marketing Date : 2010-09-15
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Bupropion manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Bupropion, including repackagers and relabelers. The FDA regulates Bupropion manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Bupropion API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Bupropion manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Bupropion supplier is an individual or a company that provides Bupropion active pharmaceutical ingredient (API) or Bupropion finished formulations upon request. The Bupropion suppliers may include Bupropion API manufacturers, exporters, distributors and traders.
click here to find a list of Bupropion suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Bupropion as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Bupropion API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture Bupropion as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain Bupropion and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Bupropion NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Bupropion suppliers with NDC on PharmaCompass.
We have 26 companies offering Bupropion
Get in contact with the supplier of your choice:
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