01 1Abbott Laboratories
02 1Guangzhou Pharmaceutical Holding Limited
03 1HEC Pharm
04 1HENAN TOPFOND PHARMACEUTICAL Co,. Ltd
05 1JIANGXI GUOYAO PHARMACEUTICAL
06 1Livzon Pharmaceutical Group
07 1NCPC HUALUAN PHARMACEUTICAL CO LTD
08 1Nanyang Pukang Pharmaceutical Co., Ltd.
09 2Ningxia Taiyicin Biotech
10 1Pfizer Inc
11 1Suzhou no. 4 Pharmaceutical Factory
12 1Xinyu Pharmaceutical
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PharmaCompass offers a list of Lincomycin 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 Lincomycin Hydrochloride manufacturer or Lincomycin Hydrochloride supplier for your needs.
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PharmaCompass also assists you with knowing the Lincomycin Hydrochloride API Price utilized in the formulation of products. Lincomycin Hydrochloride API Price is not always fixed or binding as the Lincomycin Hydrochloride Price is obtained through a variety of data sources. The Lincomycin Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A U 10149a manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of U 10149a, including repackagers and relabelers. The FDA regulates U 10149a manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. U 10149a 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 U 10149a supplier is an individual or a company that provides U 10149a active pharmaceutical ingredient (API) or U 10149a finished formulations upon request. The U 10149a suppliers may include U 10149a API manufacturers, exporters, distributors and traders.
click here to find a list of U 10149a suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A U 10149a DMF (Drug Master File) is a document detailing the whole manufacturing process of U 10149a active pharmaceutical ingredient (API) in detail. Different forms of U 10149a DMFs exist exist since differing nations have different regulations, such as U 10149a USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A U 10149a DMF submitted to regulatory agencies in the US is known as a USDMF. U 10149a USDMF includes data on U 10149a's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The U 10149a USDMF is kept confidential to protect the manufacturer’s intellectual property.
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We have 12 companies offering U 10149a
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