Malladi is a leader in Ephedrine, Pseudoephedrine Salts & Phenylephrine HCl // USFDA, EDQM, ANSM, KFDA, and TGA inspected.
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01 1M/s. Malladi Drugs & Pharmaceuticals Limited
02 1M/s Ami Lifesciences
03 1M/s. Shilpa Medicare Ltd.,
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01 1Tranexamic Acid (USP/EP/BP/IP
02 1Tranexamic Acid BP/USP/EP/JP
03 1Tranexamic Acid USP/EP
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01 1WC-0054
02 1WC-0093
03 1WC-0147
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01 3India
Malladi is a leader in Ephedrine, Pseudoephedrine Salts & Phenylephrine HCl // USFDA, EDQM, ANSM, KFDA, and TGA inspected.
Date of Issue : 2022-06-08
Valid Till : 2025-07-14
Written Confirmation Number : WC-0093
Address of the Firm : Unit-3, 7B & 7C, SICOT Industrial Complex, Ranipet 632 403, Ranipet District, Ta...
Date of Issue : 2022-08-11
Valid Till : 2025-06-26
Written Confirmation Number : WC-0054
Address of the Firm : Block No. 82/B, ECP Road, At & Post. Karakhadi, Tal-Padra, City Karakhadi -39145...
Date of Issue : 2019-07-05
Valid Till : 2022-07-02
Written Confirmation Number : WC-0147
Address of the Firm : 100% EOU, Raichur Industrial Growth Centre, Plot No. 33, 33A, 40-47, Chicksugur-...
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A CAS-1197-18-8 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CAS-1197-18-8, including repackagers and relabelers. The FDA regulates CAS-1197-18-8 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CAS-1197-18-8 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 CAS-1197-18-8 supplier is an individual or a company that provides CAS-1197-18-8 active pharmaceutical ingredient (API) or CAS-1197-18-8 finished formulations upon request. The CAS-1197-18-8 suppliers may include CAS-1197-18-8 API manufacturers, exporters, distributors and traders.
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A CAS-1197-18-8 written confirmation (CAS-1197-18-8 WC) is an official document issued by a regulatory agency to a CAS-1197-18-8 manufacturer, verifying that the manufacturing facility of a CAS-1197-18-8 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting CAS-1197-18-8 APIs or CAS-1197-18-8 finished pharmaceutical products to another nation, regulatory agencies frequently require a CAS-1197-18-8 WC (written confirmation) as part of the regulatory process.
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