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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A JUNEL FE 1/20-1 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of JUNEL FE 1/20-1, including repackagers and relabelers. The FDA regulates JUNEL FE 1/20-1 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. JUNEL FE 1/20-1 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 JUNEL FE 1/20-1 supplier is an individual or a company that provides JUNEL FE 1/20-1 active pharmaceutical ingredient (API) or JUNEL FE 1/20-1 finished formulations upon request. The JUNEL FE 1/20-1 suppliers may include JUNEL FE 1/20-1 API manufacturers, exporters, distributors and traders.
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A JUNEL FE 1/20-1 written confirmation (JUNEL FE 1/20-1 WC) is an official document issued by a regulatory agency to a JUNEL FE 1/20-1 manufacturer, verifying that the manufacturing facility of a JUNEL FE 1/20-1 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting JUNEL FE 1/20-1 APIs or JUNEL FE 1/20-1 finished pharmaceutical products to another nation, regulatory agencies frequently require a JUNEL FE 1/20-1 WC (written confirmation) as part of the regulatory process.
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