01 Abbott Laboratories (1)
02 Albion (1)
03 Bristol Myers Squibb (1)
04 Eli Lilly (1)
05 Intermountain Healthcare (1)
06 Merck & Co (1)
07 Tianjin Weijie Pharmaceutical Co., Ltd. (1)
08 Wyeth Pharmaceuticals Inc (1)
09 Blank (9)
01 DIETHYLENESTILBESTROL INTERMEDIATE PREMIXES (VET) (1)
02 DIETHYLSTILBESTROL (1)
03 DIETHYLSTILBESTROL (VET) (1)
04 DIETHYLSTILBESTROL TRADE NAME: RUMESTROL "1" AND "2" (VET) (1)
05 DIETHYLSTILBESTROL IMPLANTATION PELLETS (1)
06 DIETHYLSTILBESTROL INTERMEDIATE PREMIXES (VET) (1)
07 DIETHYLSTILBESTROL INTERMEDIATE PREMIXES (VET) (5)
08 DIETHYLSTILBESTROL INTERMEDIATE PREMIXES -STILBOSOL (VET) (1)
09 DIETHYLSTILBESTROL INTERMEDIATE PREMIXES (VET) (1)
10 DIETHYLSTILBESTROL PWD & DIETHYLSTILBESTROL 50% SUSPEN. IN SOYBEAN OIL (1)
11 GR OF DIETHYLSTILBESTROL INTERMEDIATE PREMIXES (VET) (1)
12 STILBETIN SUPPLEMENT 50 (DIETHYLSTILBESTROL IN POLYETHYLENE GLYCOL) (1)
13 TAPAZOLE AND DIETHYLSTILBESTROL FOR CATTLE (VET) (1)
01 China (1)
02 Japan (1)
03 U.S.A (6)
04 Blank (9)
01 Active (1)
02 Inactive (16)
01 Blank (17)
73
PharmaCompass offers a list of Diethylstilbestrol 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 Diethylstilbestrol manufacturer or Diethylstilbestrol supplier for your needs.
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A MolPort-001-785-868 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MolPort-001-785-868, including repackagers and relabelers. The FDA regulates MolPort-001-785-868 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MolPort-001-785-868 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A MolPort-001-785-868 supplier is an individual or a company that provides MolPort-001-785-868 active pharmaceutical ingredient (API) or MolPort-001-785-868 finished formulations upon request. The MolPort-001-785-868 suppliers may include MolPort-001-785-868 API manufacturers, exporters, distributors and traders.
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A MolPort-001-785-868 DMF (Drug Master File) is a document detailing the whole manufacturing process of MolPort-001-785-868 active pharmaceutical ingredient (API) in detail. Different forms of MolPort-001-785-868 DMFs exist exist since differing nations have different regulations, such as MolPort-001-785-868 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A MolPort-001-785-868 DMF submitted to regulatory agencies in the US is known as a USDMF. MolPort-001-785-868 USDMF includes data on MolPort-001-785-868's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The MolPort-001-785-868 USDMF is kept confidential to protect the manufacturer’s intellectual property.
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