TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
01 1M/s Teva API India Private Limited
02 1M/s Maithri Drugs Private Limited
03 1M/s Divi's Laboratories Limited
01 1Carbidopa IP/USP/Ph.Eur/BP
02 1Carbidopa USP
03 1Carbidopa USP/Ph.Eur/IH
01 1WC-0002
02 1WC-0030n
03 1WC-0407
01 3India
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
Date of Issue : 2025-04-24
Valid Till : 2028-05-25
Written Confirmation Number : WC-0002
Address of the Firm : Plot No. A-2, A-2/1, A-/2, UPSIDC Industrial Area, Bijnor Road, Gajraula -244235...
Maithri Drugs: Delivering Trusted, High-Quality APIs to 35+ Countries with Innovation, Compliance, and Excellence.
Date of Issue : 2024-02-12
Valid Till : 2027-02-11
Written Confirmation Number : WC-0407
Address of the Firm : Sy. No. 205, 222 to 226, IDA Bonthapally, Bonthapally (Village), Gummadidala (Ma...
Date of Issue : 2022-06-03
Valid Till : 2025-06-16
Written Confirmation Number : WC-0030n
Address of the Firm : UNIT-II, Annavaram (Post), Chippada Village, Bheemunipatnam Mandai, Visakhapatna...
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PharmaCompass offers a list of Carbidopa 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 Carbidopa manufacturer or Carbidopa supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Carbidopa manufacturer or Carbidopa supplier.
PharmaCompass also assists you with knowing the Carbidopa API Price utilized in the formulation of products. Carbidopa API Price is not always fixed or binding as the Carbidopa Price is obtained through a variety of data sources. The Carbidopa Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A EU-0100382 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of EU-0100382, including repackagers and relabelers. The FDA regulates EU-0100382 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. EU-0100382 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 EU-0100382 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A EU-0100382 supplier is an individual or a company that provides EU-0100382 active pharmaceutical ingredient (API) or EU-0100382 finished formulations upon request. The EU-0100382 suppliers may include EU-0100382 API manufacturers, exporters, distributors and traders.
click here to find a list of EU-0100382 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A EU-0100382 written confirmation (EU-0100382 WC) is an official document issued by a regulatory agency to a EU-0100382 manufacturer, verifying that the manufacturing facility of a EU-0100382 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting EU-0100382 APIs or EU-0100382 finished pharmaceutical products to another nation, regulatory agencies frequently require a EU-0100382 WC (written confirmation) as part of the regulatory process.
click here to find a list of EU-0100382 suppliers with Written Confirmation (WC) on PharmaCompass.
We have 3 companies offering EU-0100382
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