01 3Cipla Limited
02 2Cipla Limited.
03 1F. Hoffmann-La Roche Ltd
04 1Jeil Pharmaceutical Co., Ltd.
05 1Kyungbo Pharmaceutical Co., Ltd.
06 1MSN Laboratories Private Limited
07 1Mexico City SA De CV
08 1Natco Pharma Ltd., Chemical Division
09 1Shilpa Pharma Lifesciences Limited
10 1Sicor de Mexico SA de CV
11 1Uquifa Mexico SA of CV
22
PharmaCompass offers a list of Erlotinib 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 Erlotinib Hydrochloride manufacturer or Erlotinib Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Erlotinib Hydrochloride manufacturer or Erlotinib Hydrochloride supplier.
PharmaCompass also assists you with knowing the Erlotinib Hydrochloride API Price utilized in the formulation of products. Erlotinib Hydrochloride API Price is not always fixed or binding as the Erlotinib Hydrochloride Price is obtained through a variety of data sources. The Erlotinib Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Erlotinib Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Erlotinib Hydrochloride, including repackagers and relabelers. The FDA regulates Erlotinib Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Erlotinib 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.
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A Erlotinib Hydrochloride supplier is an individual or a company that provides Erlotinib Hydrochloride active pharmaceutical ingredient (API) or Erlotinib Hydrochloride finished formulations upon request. The Erlotinib Hydrochloride suppliers may include Erlotinib Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Erlotinib Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price 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 Erlotinib Hydrochloride Drug Master File in Korea (Erlotinib Hydrochloride KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Erlotinib Hydrochloride. The MFDS reviews the Erlotinib Hydrochloride KDMF as part of the drug registration process and uses the information provided in the Erlotinib Hydrochloride KDMF to evaluate the safety and efficacy of the drug.
After submitting a Erlotinib Hydrochloride 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 Erlotinib Hydrochloride API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Erlotinib Hydrochloride suppliers with KDMF on PharmaCompass.
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