01 1Zydus Lifesciences Limited
01 1Handok Co., Ltd.
01 1tirofiban hydrochloride hydrate
01 1India
tirofiban hydrochloride hydrate
Registrant Name : Handok Co., Ltd.
Registration Date : 2013-08-28
Registration Number : Su130-3-ND
Manufacturer Name : Zydus Lifesciences Limited
Manufacturer Address : Plot No. 26 to 29 & 31, Umraya Road, Dabhasa, Tal-Padra, City : Dabhasa-391 440, Dist...
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PharmaCompass offers a list of Tirofiban Hydrochloride Monohydrate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Tirofiban Hydrochloride Monohydrate manufacturer or Tirofiban Hydrochloride Monohydrate supplier for your needs.
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A Tirofiban Hydrochloride Monohydrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tirofiban Hydrochloride Monohydrate, including repackagers and relabelers. The FDA regulates Tirofiban Hydrochloride Monohydrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tirofiban Hydrochloride Monohydrate 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 Tirofiban Hydrochloride Monohydrate supplier is an individual or a company that provides Tirofiban Hydrochloride Monohydrate active pharmaceutical ingredient (API) or Tirofiban Hydrochloride Monohydrate finished formulations upon request. The Tirofiban Hydrochloride Monohydrate suppliers may include Tirofiban Hydrochloride Monohydrate API manufacturers, exporters, distributors and traders.
click here to find a list of Tirofiban Hydrochloride Monohydrate suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Tirofiban Hydrochloride Monohydrate Drug Master File in Korea (Tirofiban Hydrochloride Monohydrate KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Tirofiban Hydrochloride Monohydrate. The MFDS reviews the Tirofiban Hydrochloride Monohydrate KDMF as part of the drug registration process and uses the information provided in the Tirofiban Hydrochloride Monohydrate KDMF to evaluate the safety and efficacy of the drug.
After submitting a Tirofiban Hydrochloride Monohydrate KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their Tirofiban Hydrochloride Monohydrate API can apply through the Korea Drug Master File (KDMF).
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