01 1M/s Zydus Takeda Healthcare Pvt. Ltd.
02 1M/sZyus Takeda Healthcare pvt ltd
01 1Urapidil IH/ Urapidil Hydrochloride IH
02 1Urapidil IH/Urapidil Hydrochloride IH
01 1WC-0204
02 1WC-204
01 2India
Urapidil IH/ Urapidil Hydrochloride IH
Date of Issue : 2023-06-23
Valid Till : 2025-07-07
Written Confirmation Number : WC-0204
Address of the Firm : C-4, MIDC, Village Pawne, Thane Belapur Road,\r\nVashi, Navi Mumbai — 400 703
Urapidil IH/Urapidil Hydrochloride IH
Date of Issue : 2022-06-15
Valid Till : 2025-07-07
Written Confirmation Number : WC-204
Address of the Firm : C-4 Thane, MIDC,belapur road, Vashi, Navi Mumbai,Maharastra, India
A Urapidil Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Urapidil Hydrochloride, including repackagers and relabelers. The FDA regulates Urapidil Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Urapidil Hydrochloride API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Urapidil Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Urapidil Hydrochloride supplier is an individual or a company that provides Urapidil Hydrochloride active pharmaceutical ingredient (API) or Urapidil Hydrochloride finished formulations upon request. The Urapidil Hydrochloride suppliers may include Urapidil Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Urapidil Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Urapidil Hydrochloride written confirmation (Urapidil Hydrochloride WC) is an official document issued by a regulatory agency to a Urapidil Hydrochloride manufacturer, verifying that the manufacturing facility of a Urapidil Hydrochloride active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Urapidil Hydrochloride APIs or Urapidil Hydrochloride finished pharmaceutical products to another nation, regulatory agencies frequently require a Urapidil Hydrochloride WC (written confirmation) as part of the regulatory process.
click here to find a list of Urapidil Hydrochloride suppliers with Written Confirmation (WC) on PharmaCompass.
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