A (3S,4R)-Cabastine Hydrochloride DMF (Drug Master File) is a document detailing the whole manufacturing process of (3S,4R)-Cabastine Hydrochloride active pharmaceutical ingredient (API) in detail. Different forms of (3S,4R)-Cabastine Hydrochloride DMFs exist exist since differing nations have different regulations, such as (3S,4R)-Cabastine Hydrochloride USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A (3S,4R)-Cabastine Hydrochloride DMF submitted to regulatory agencies in the US is known as a USDMF. (3S,4R)-Cabastine Hydrochloride USDMF includes data on (3S,4R)-Cabastine Hydrochloride's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The (3S,4R)-Cabastine Hydrochloride USDMF is kept confidential to protect the manufacturer’s intellectual property.
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