01 1M/s Apothecon Pharmaceuticals Pvt ltd
01 1Nicardipine Hydrochloride USP
01 1WC-0369A7
01 1India
Date of Issue : 2022-09-01
Valid Till : 2022-09-08
Written Confirmation Number : WC-0369A7
Address of the Firm : Plot No 1134,1135,1136,1137, 1143B, 1144 A & B,1138 A & B, Padra Jambusar Highwa...
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PharmaCompass offers a list of Nicardipine Hydrochloride 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 Nicardipine Hydrochloride manufacturer or Nicardipine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Nicardipine Hydrochloride manufacturer or Nicardipine Hydrochloride supplier.
PharmaCompass also assists you with knowing the Nicardipine Hydrochloride API Price utilized in the formulation of products. Nicardipine Hydrochloride API Price is not always fixed or binding as the Nicardipine Hydrochloride Price is obtained through a variety of data sources. The Nicardipine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A N0635 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of N0635, including repackagers and relabelers. The FDA regulates N0635 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. N0635 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 N0635 supplier is an individual or a company that provides N0635 active pharmaceutical ingredient (API) or N0635 finished formulations upon request. The N0635 suppliers may include N0635 API manufacturers, exporters, distributors and traders.
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A N0635 written confirmation (N0635 WC) is an official document issued by a regulatory agency to a N0635 manufacturer, verifying that the manufacturing facility of a N0635 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting N0635 APIs or N0635 finished pharmaceutical products to another nation, regulatory agencies frequently require a N0635 WC (written confirmation) as part of the regulatory process.
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