01 1M/s. Cadila Pharmaceuticals Ltd.,
02 1M/s. Lupin Limited.,
03 1M/s. Lupin Ltd
01 1Ethambutol HCL (Ph. Eur./BP/USP)
02 1Ethambutol Hydrochloride USP/EP
03 1Ethambutol Hydrochloride USP/EP/BP
01 1WC-0048
02 1WC-0074
03 1WC-0201
01 3India
Ethambutol HCL (Ph. Eur./BP/USP)
Date of Issue : 2022-09-01
Valid Till : 2025-07-02
Written Confirmation Number : WC-0074
Address of the Firm : 294, GIDC Estate, Ankleshwar-393 002, Bharuch, Gujarat, India
Ethambutol Hydrochloride USP/EP
Date of Issue : 2022-09-30
Valid Till : 2025-09-10
Written Confirmation Number : WC-0201
Address of the Firm : T-142, MIDC, Tarapur, Vil: Boisar, Dist: Thane-401 506, Maharashtra State
Ethambutol Hydrochloride USP/EP/BP
Date of Issue : 2019-08-01
Valid Till : 2022-07-31
Written Confirmation Number : WC-0048
Address of the Firm : 124, GIDC Estate, Ankleshwar-393 002, Gujarat
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PharmaCompass offers a list of Ethambutol Dihydrochloride 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 Ethambutol Dihydrochloride manufacturer or Ethambutol Dihydrochloride supplier for your needs.
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PharmaCompass also assists you with knowing the Ethambutol Dihydrochloride API Price utilized in the formulation of products. Ethambutol Dihydrochloride API Price is not always fixed or binding as the Ethambutol Dihydrochloride Price is obtained through a variety of data sources. The Ethambutol Dihydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Ethambutol Dihydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ethambutol Dihydrochloride, including repackagers and relabelers. The FDA regulates Ethambutol Dihydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ethambutol Dihydrochloride 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 Ethambutol Dihydrochloride supplier is an individual or a company that provides Ethambutol Dihydrochloride active pharmaceutical ingredient (API) or Ethambutol Dihydrochloride finished formulations upon request. The Ethambutol Dihydrochloride suppliers may include Ethambutol Dihydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Ethambutol Dihydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Ethambutol Dihydrochloride written confirmation (Ethambutol Dihydrochloride WC) is an official document issued by a regulatory agency to a Ethambutol Dihydrochloride manufacturer, verifying that the manufacturing facility of a Ethambutol Dihydrochloride active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Ethambutol Dihydrochloride APIs or Ethambutol Dihydrochloride finished pharmaceutical products to another nation, regulatory agencies frequently require a Ethambutol Dihydrochloride WC (written confirmation) as part of the regulatory process.
click here to find a list of Ethambutol Dihydrochloride suppliers with Written Confirmation (WC) on PharmaCompass.
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