Neuland Laboratories- A dedicated 100% API provider.
01 1M/sNeuland Laboratories ltd
02 1M/s. Godavari Drugs Limited
03 1M/sSun Pharmaceutical Industries Ltd
01 1Ciprofloxacin BP/USP/EP
02 1Ciprofloxacin Ph. Eur
03 1Ciprofloxacin USP/Ph. Eur
01 1WC-0037
02 1WC-0216
03 1WC-0628
01 3India
Neuland Laboratories- A dedicated 100% API provider.
Date of Issue : 2025-06-27
Valid Till : 2028-06-16
Written Confirmation Number : WC-0037
Address of the Firm : Unit-ll, Plot No. 92-94, 257-259, IDA Pashamylaram, Pashamylaram Village, Patanc...
Date of Issue : 2025-11-28
Valid Till : 2028-11-27
Written Confirmation Number : WC-0628
Address of the Firm : A-6/2, MIDC, Nanded -431603, Taluka: Nanded, District: Nanded, Maharashtra, Indi...
Date of Issue : 2025-07-10
Valid Till : 2028-07-04
Written Confirmation Number : WC-0216
Address of the Firm : Industrial Area-03, A. B. Road, Dewas
96
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A C17H18FN3O3 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of C17H18FN3O3, including repackagers and relabelers. The FDA regulates C17H18FN3O3 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. C17H18FN3O3 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 C17H18FN3O3 supplier is an individual or a company that provides C17H18FN3O3 active pharmaceutical ingredient (API) or C17H18FN3O3 finished formulations upon request. The C17H18FN3O3 suppliers may include C17H18FN3O3 API manufacturers, exporters, distributors and traders.
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A C17H18FN3O3 written confirmation (C17H18FN3O3 WC) is an official document issued by a regulatory agency to a C17H18FN3O3 manufacturer, verifying that the manufacturing facility of a C17H18FN3O3 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting C17H18FN3O3 APIs or C17H18FN3O3 finished pharmaceutical products to another nation, regulatory agencies frequently require a C17H18FN3O3 WC (written confirmation) as part of the regulatory process.
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