01 1CTX LIFESCIENCES PRIVATE LIMITED
02 1M/s Sai Supreme Chemicals
03 1M/s. CTX Life Sciences Pvt. Ltd.,
04 1M/s. IPCA Laboratories Ltd.,
01 1Propanolol Hydrochloride (BP/USP/ Ph.Eur/JP)
02 1Propanolol hydrochloride BP/EP/USP
03 2Propranolol Hydrochloride EP/USP
01 1WC-0091
02 1WC-0097
03 1WC-0097A3
04 1WC-0514
01 4India
Propranolol Hydrochloride EP/USP
Date of Issue : 2022-06-24
Valid Till : 2025-07-02
Written Confirmation Number : WC-0097
Address of the Firm : Block No. 251/P, 252/P, 253 to 255, 256/P,258/P, 276/P, 277/P, 278/P, 279 To 282...
Propranolol Hydrochloride EP/USP
Date of Issue : 2019-09-27
Valid Till : 2022-07-02
Written Confirmation Number : WC-0097A3
Address of the Firm : Block No. 251/P, 252/P, 253 to 255, 256/P,258/P, 276/P, 277/P, 278/P, 279 To 282...
Propanolol Hydrochloride (BP/USP/ Ph.Eur/JP)
Date of Issue : 2022-06-08
Valid Till : 2025-07-02
Written Confirmation Number : WC-0091
Address of the Firm : Sejavta, Ratlam, Madhya Pradesh
Propanolol hydrochloride BP/EP/USP
Date of Issue : 2021-12-01
Valid Till : 2024-11-30
Written Confirmation Number : WC-0514
Address of the Firm : Plot No F-7, Sipcot Industrial Complex,Gummidipoondi, Thiruvallur, Tamil Nadu-60...
A Scandrug manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Scandrug, including repackagers and relabelers. The FDA regulates Scandrug manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Scandrug 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 Scandrug supplier is an individual or a company that provides Scandrug active pharmaceutical ingredient (API) or Scandrug finished formulations upon request. The Scandrug suppliers may include Scandrug API manufacturers, exporters, distributors and traders.
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A Scandrug written confirmation (Scandrug WC) is an official document issued by a regulatory agency to a Scandrug manufacturer, verifying that the manufacturing facility of a Scandrug active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Scandrug APIs or Scandrug finished pharmaceutical products to another nation, regulatory agencies frequently require a Scandrug WC (written confirmation) as part of the regulatory process.
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