01 M/s Aurore Pharmaceuticals Private Limited (2)
02 M/s Mangalam Drugs and Organics Ltd (1)
03 M/s Sterile India Pvt Ltd (1)
04 M/s Vital Laboratories Private limited Plant-I (1)
05 M/s Vital Laboratories Pvt Ltd (1)
06 M/s. Great Pacific Exports Pvt. Ltd. (1)
07 M/s. Hetero Drugs Limited., (1)
08 M/s. Mac-Chem Products (India) Pvt. Ltd (1)
09 M/s. Mangalam Drugs & Organics Ltd., Unit-2 (1)
10 M/s. Mylan Laboratories Ltd., (1)
11 M/s. Piramal Enterprises Limited (1)
12 M/s. Suven Life Sciences Limited (1)
01 Aciclovir (Ph. Eur.)/USP (1)
02 Aciclovir BP/EP/USP (1)
03 Aciclovir EP (1)
04 Aciclovir EP/BP/USP (1)
05 Aciclovir EP/IP (1)
06 Aciclovir sodium sterile IH (1)
07 Acyclovir (2)
08 Acyclovir (BP/Ph. Eur./USP) (1)
09 Acyclovir (USP) (1)
10 Acyclovir (USP/Ph. Eur.) (1)
11 Acyclovir USP (1)
12 Acyclovir USP, Ph.Eur (1)
01 WC-0042 (1)
02 WC-0066 (1)
03 WC-0117 (1)
04 WC-0119 (1)
05 WC-0119A9 (1)
06 WC-0123 (1)
07 WC-0167 (1)
08 WC-0275 (1)
09 WC-0303A2 (1)
10 WC-0303n (1)
11 WC-0378A2 (1)
12 WC-0473 (1)
13 WC-247 (1)
01 India (13)
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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 written confirmation (MolPort-001-889-834 WC) is an official document issued by a regulatory agency to a MolPort-001-889-834 manufacturer, verifying that the manufacturing facility of a MolPort-001-889-834 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting MolPort-001-889-834 APIs or MolPort-001-889-834 finished pharmaceutical products to another nation, regulatory agencies frequently require a MolPort-001-889-834 WC (written confirmation) as part of the regulatory process.
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We have 10 companies offering MolPort-001-889-834
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