01 Ajinomoto OmniChem N.V. (1)
02 AstraZeneca (1)
03 Aurore Life Sciences (2)
04 Charioteer (1)
05 Cipla (1)
06 Hetero Drugs (1)
07 Hubei Yitai Pharmaceutical Co. , Ltd. (1)
08 Livzon Group Fuzhou Fuxing Pharmaceutical Co., Ltd. (1)
09 Mallinckrodt Pharmaceuticals (2)
10 Olon S.p.A (2)
11 Piramal Pharma Solutions (1)
12 Qidong Dongyue Pharmaceutical Co., Ltd. (1)
13 Quimica Sintetica S.A. (1)
14 RANBAXY LABORATORIES LIMITED (1)
15 Recordati (1)
16 ST Pharma (1)
17 Signa S.A. de C.V. (1)
18 Teva API (4)
19 UQUIFA (1)
20 Viatris (1)
21 YUNG ZIP CHEMICAL INDUSTRIAL (2)
22 Zhejiang Zhebei Pharmaceutical (1)
23 Blank (3)
01 ACYCLOVIR (16)
02 ACYCLOVIR (NON-STERILE, BULK FORM) (1)
03 ACYCLOVIR (PROCESS II) (1)
04 ACYCLOVIR ACTIVE SUBSTANCE (1)
05 ACYCLOVIR DRUG SUBSTANCE (2)
06 ACYCLOVIR USP (6)
07 ACYCLOVIR USP (API) (1)
08 ACYCLOVIR USP (MICRONIZED), CODED 2524 (1)
09 ACYCLOVIR USP [SITE KHAZIPALLY] (1)
10 ACYCLOVIR USP, BULK (1)
11 ACYCLOVIR, USP (1)
01 Belgium (1)
02 China (5)
03 India (5)
04 Ireland (2)
05 Israel (4)
06 Italy (3)
07 Mexico (1)
08 South Korea (1)
09 Spain (2)
10 Taiwan (2)
11 U.S.A (2)
12 United Kingdom (1)
13 Blank (3)
01 Active (18)
02 Inactive (14)
01 Complete (14)
02 Blank (18)
59
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A MolPort-001-889-834 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MolPort-001-889-834, including repackagers and relabelers. The FDA regulates MolPort-001-889-834 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MolPort-001-889-834 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-001-889-834 supplier is an individual or a company that provides MolPort-001-889-834 active pharmaceutical ingredient (API) or MolPort-001-889-834 finished formulations upon request. The MolPort-001-889-834 suppliers may include MolPort-001-889-834 API manufacturers, exporters, distributors and traders.
click here to find a list of MolPort-001-889-834 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A MolPort-001-889-834 DMF (Drug Master File) is a document detailing the whole manufacturing process of MolPort-001-889-834 active pharmaceutical ingredient (API) in detail. Different forms of MolPort-001-889-834 DMFs exist exist since differing nations have different regulations, such as MolPort-001-889-834 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A MolPort-001-889-834 DMF submitted to regulatory agencies in the US is known as a USDMF. MolPort-001-889-834 USDMF includes data on MolPort-001-889-834's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The MolPort-001-889-834 USDMF is kept confidential to protect the manufacturer’s intellectual property.
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We have 22 companies offering MolPort-001-889-834
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