01 1M/s Naari Pharma Private Limited
02 1M/s. Indo Phyto Chemicals Pvt. Ltd.
01 1Norethisterone Enanthate IH
02 1Norethisterone enantate IH
01 1WC-0297
02 1WC-297
01 2India
Date of Issue : 2018-11-05
Valid Till : 2021-11-04
Written Confirmation Number : WC-297
Address of the Firm : Village Shankarpur, P.O-Pirumadara, Tehsil Ramnagar, Distt-Nanital, Uttarakhand-...
Date of Issue : 2022-09-01
Valid Till : 2024-11-05
Written Confirmation Number : WC-0297
Address of the Firm : Village-Sakhanpur, Po-Pirumadara-244715\r\nTehsil-Ramnager, Dist- Nainital, Utta...
A Norethisterone Enanthate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Norethisterone Enanthate, including repackagers and relabelers. The FDA regulates Norethisterone Enanthate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Norethisterone Enanthate 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 Norethisterone Enanthate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Norethisterone Enanthate supplier is an individual or a company that provides Norethisterone Enanthate active pharmaceutical ingredient (API) or Norethisterone Enanthate finished formulations upon request. The Norethisterone Enanthate suppliers may include Norethisterone Enanthate API manufacturers, exporters, distributors and traders.
click here to find a list of Norethisterone Enanthate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Norethisterone Enanthate written confirmation (Norethisterone Enanthate WC) is an official document issued by a regulatory agency to a Norethisterone Enanthate manufacturer, verifying that the manufacturing facility of a Norethisterone Enanthate active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Norethisterone Enanthate APIs or Norethisterone Enanthate finished pharmaceutical products to another nation, regulatory agencies frequently require a Norethisterone Enanthate WC (written confirmation) as part of the regulatory process.
click here to find a list of Norethisterone Enanthate suppliers with Written Confirmation (WC) on PharmaCompass.
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