01 1GVK Biosciences Private Limited
02 1M/s Biosciences
03 1M/s. Sun Pharmaceuticals Industries Ltd.
01 1Dobutamine HCI (USP/Ph. Eur)
02 1Dobutamine HCl USP
03 1Dobutamine Hydrochloride (USP/EP/BP/JP)
01 1WC-0124
02 1WC-0124A2
03 1WC-0159
01 3India
Date of Issue : 2019-10-31
Valid Till : 2022-07-02
Written Confirmation Number : WC-0124
Address of the Firm : Plot No.28 A, IDA, Nacharam, Hyderabad, AP
Date of Issue : 2020-08-07
Valid Till : 2022-07-02
Written Confirmation Number : WC-0124A2
Address of the Firm : Plot No.28 A, IDA, Nacharam,telangana,India \r\n
Dobutamine Hydrochloride (USP/EP/BP/JP)
Date of Issue : 2022-06-08
Valid Till : 2025-07-25
Written Confirmation Number : WC-0159
Address of the Firm : A-7/A-8, MIDC, Ahmednagar-414 111, Maharashtra State
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PharmaCompass offers a list of Dobutamine 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 Dobutamine Hydrochloride manufacturer or Dobutamine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Dobutamine Hydrochloride manufacturer or Dobutamine Hydrochloride supplier.
PharmaCompass also assists you with knowing the Dobutamine Hydrochloride API Price utilized in the formulation of products. Dobutamine Hydrochloride API Price is not always fixed or binding as the Dobutamine Hydrochloride Price is obtained through a variety of data sources. The Dobutamine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Dobutamine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dobutamine, including repackagers and relabelers. The FDA regulates Dobutamine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dobutamine 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 Dobutamine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Dobutamine supplier is an individual or a company that provides Dobutamine active pharmaceutical ingredient (API) or Dobutamine finished formulations upon request. The Dobutamine suppliers may include Dobutamine API manufacturers, exporters, distributors and traders.
click here to find a list of Dobutamine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Dobutamine written confirmation (Dobutamine WC) is an official document issued by a regulatory agency to a Dobutamine manufacturer, verifying that the manufacturing facility of a Dobutamine active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Dobutamine APIs or Dobutamine finished pharmaceutical products to another nation, regulatory agencies frequently require a Dobutamine WC (written confirmation) as part of the regulatory process.
click here to find a list of Dobutamine suppliers with Written Confirmation (WC) on PharmaCompass.
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