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01 1M/sIPCA Laboratories Limited
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01 1Norethisterone Acetate Ph. Eur/BP
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01 1WC-0402A2
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01 1India
Norethisterone Acetate Ph. Eur/BP
Date of Issue : 2020-07-06
Valid Till : 2023-05-24
Written Confirmation Number : WC-0402A2
Address of the Firm : Plot No. 23-24, GIDC Estate, Nandesari-391 340, Dist. Vadodara, Gujarat, India
89
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A LO LOESTRIN FE-1 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of LO LOESTRIN FE-1, including repackagers and relabelers. The FDA regulates LO LOESTRIN FE-1 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. LO LOESTRIN FE-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 LO LOESTRIN FE-1 supplier is an individual or a company that provides LO LOESTRIN FE-1 active pharmaceutical ingredient (API) or LO LOESTRIN FE-1 finished formulations upon request. The LO LOESTRIN FE-1 suppliers may include LO LOESTRIN FE-1 API manufacturers, exporters, distributors and traders.
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A LO LOESTRIN FE-1 written confirmation (LO LOESTRIN FE-1 WC) is an official document issued by a regulatory agency to a LO LOESTRIN FE-1 manufacturer, verifying that the manufacturing facility of a LO LOESTRIN FE-1 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting LO LOESTRIN FE-1 APIs or LO LOESTRIN FE-1 finished pharmaceutical products to another nation, regulatory agencies frequently require a LO LOESTRIN FE-1 WC (written confirmation) as part of the regulatory process.
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