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 Norethindrone Enanthate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Norethindrone Enanthate, including repackagers and relabelers. The FDA regulates Norethindrone Enanthate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Norethindrone 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 Norethindrone Enanthate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Norethindrone Enanthate supplier is an individual or a company that provides Norethindrone Enanthate active pharmaceutical ingredient (API) or Norethindrone Enanthate finished formulations upon request. The Norethindrone Enanthate suppliers may include Norethindrone Enanthate API manufacturers, exporters, distributors and traders.
click here to find a list of Norethindrone Enanthate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Norethindrone Enanthate written confirmation (Norethindrone Enanthate WC) is an official document issued by a regulatory agency to a Norethindrone Enanthate manufacturer, verifying that the manufacturing facility of a Norethindrone Enanthate active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Norethindrone Enanthate APIs or Norethindrone Enanthate finished pharmaceutical products to another nation, regulatory agencies frequently require a Norethindrone Enanthate WC (written confirmation) as part of the regulatory process.
click here to find a list of Norethindrone Enanthate suppliers with Written Confirmation (WC) on PharmaCompass.
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