01 1M/s Naari Pharma Private Limited
02 1M/s. Indo Phyto Chemicals Pvt. Ltd.
03 1M/sIPCA Laboratories Limited
01 1Norethisteron acetate BP
02 1Norethisterone Acetate BP/USP/EP
03 1norethisterone acetate EP/BP
01 1WC-0297
02 1WC-0402A2
03 1WC-297
01 3India
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 : 2020-09-08
Valid Till : 2023-04-24
Written Confirmation Number : WC-0402A2
Address of the Firm : Plot no. 23-24 GIDC Estate Nandesari-391340 Dist Vadodara Gujarat
Norethisterone Acetate BP/USP/EP
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...
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PharmaCompass offers a list of Norethisterone Acetate 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 Norethisterone Acetate manufacturer or Norethisterone Acetate supplier for your needs.
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PharmaCompass also assists you with knowing the Norethisterone Acetate API Price utilized in the formulation of products. Norethisterone Acetate API Price is not always fixed or binding as the Norethisterone Acetate Price is obtained through a variety of data sources. The Norethisterone Acetate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A LO-BLISOVI FE manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of LO-BLISOVI FE, including repackagers and relabelers. The FDA regulates LO-BLISOVI FE manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. LO-BLISOVI FE 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 LO-BLISOVI FE supplier is an individual or a company that provides LO-BLISOVI FE active pharmaceutical ingredient (API) or LO-BLISOVI FE finished formulations upon request. The LO-BLISOVI FE suppliers may include LO-BLISOVI FE API manufacturers, exporters, distributors and traders.
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A LO-BLISOVI FE written confirmation (LO-BLISOVI FE WC) is an official document issued by a regulatory agency to a LO-BLISOVI FE manufacturer, verifying that the manufacturing facility of a LO-BLISOVI FE active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting LO-BLISOVI FE APIs or LO-BLISOVI FE finished pharmaceutical products to another nation, regulatory agencies frequently require a LO-BLISOVI FE WC (written confirmation) as part of the regulatory process.
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