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Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives. 
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01 Aarti Pharmalabs (1)
02 Supriya Lifescience (1)
03 Alembic Pharmaceuticals Limited (1)
04 Aurobindo Pharma Limited (1)
05 Cadila Pharmaceuticals (1)
06 Chemeca Drugs (1)
07 Chemi SpA (2)
08 Cilag AG (1)
09 Derivados Quimicos SAU (1)
10 Dipharma (1)
11 Divis Laboratories (1)
12 Erregierre SpA (1)
13 Glenmark Life Sciences (1)
14 Granules India Limited (1)
15 HANZHONG HANJIANG VENTUREPHARM PHARMACEUTICAL LTD (1)
16 Hetero Drugs (2)
17 Hikal (2)
18 Jubilant Generics (1)
19 Lupin Ltd (1)
20 NORDIC SYNTHESIS AB (1)
21 Olon S.p.A (1)
22 Seven Star Pharmaceutical (1)
23 Sifavitor srl (1)
24 Solmag (1)
25 Sun Pharmaceutical Industries Limited (1)
26 UQUIFA (1)
27 ZHEJIANG LANGHUA PHARMACEUTICAL CO., LTD. (1)
28 Zhejiang Apeloa Jiayuan Pharmaceutical (1)
29 Zhejiang Shaxing Pharm. & Chem.Co., Ltd. (1)
30 Zhejiang Supor Pharmaceuticals Co., LTD (2)
31 Zydus Lifesciences (2)
01 BUPRIOPION HYDROCHLORIDE USP (1)
02 BUPROPION HCL (1)
03 BUPROPION HCL FV3307 (1)
04 BUPROPION HYDROCHLORIDE (13)
05 BUPROPION HYDROCHLORIDE (PROCESS-II) (1)
06 BUPROPION HYDROCHLORIDE USP (17)
07 BUPROPION HYDROCHLORIDE USP (PROCESS-II) (1)
08 BUPROPION HYDROCHLORIDE USP [PROCESS-2] (1)
01 China (6)
02 India (18)
03 Italy (7)
04 Spain (2)
05 Sweden (1)
06 Switzerland (1)
07 Taiwan (1)
01 Active (24)
02 Inactive (12)
01 Complete (17)
02 Blank (19)
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PharmaCompass offers a list of Bupropion Hydrochloride API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Bupropion Hydrochloride manufacturer or Bupropion Hydrochloride supplier for your needs.
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A MolPort-001-759-083 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MolPort-001-759-083, including repackagers and relabelers. The FDA regulates MolPort-001-759-083 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MolPort-001-759-083 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A MolPort-001-759-083 supplier is an individual or a company that provides MolPort-001-759-083 active pharmaceutical ingredient (API) or MolPort-001-759-083 finished formulations upon request. The MolPort-001-759-083 suppliers may include MolPort-001-759-083 API manufacturers, exporters, distributors and traders.
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A MolPort-001-759-083 DMF (Drug Master File) is a document detailing the whole manufacturing process of MolPort-001-759-083 active pharmaceutical ingredient (API) in detail. Different forms of MolPort-001-759-083 DMFs exist exist since differing nations have different regulations, such as MolPort-001-759-083 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A MolPort-001-759-083 DMF submitted to regulatory agencies in the US is known as a USDMF. MolPort-001-759-083 USDMF includes data on MolPort-001-759-083's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The MolPort-001-759-083 USDMF is kept confidential to protect the manufacturer’s intellectual property.
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We have 31 companies offering MolPort-001-759-083
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