01 1Patel Chem Specialties
01 1RHEOLLOSE®- CARBOXYMETHYLCELLULOSE SODIUM IP/JP/BP/EP/USP-NF
01 1India
01 1Active
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 33401
Submission : 2018-12-19
Status : Active
Type : IV
A 9004-32-4 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 9004-32-4, including repackagers and relabelers. The FDA regulates 9004-32-4 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 9004-32-4 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 9004-32-4 supplier is an individual or a company that provides 9004-32-4 active pharmaceutical ingredient (API) or 9004-32-4 finished formulations upon request. The 9004-32-4 suppliers may include 9004-32-4 API manufacturers, exporters, distributors and traders.
click here to find a list of 9004-32-4 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A 9004-32-4 DMF (Drug Master File) is a document detailing the whole manufacturing process of 9004-32-4 active pharmaceutical ingredient (API) in detail. Different forms of 9004-32-4 DMFs exist exist since differing nations have different regulations, such as 9004-32-4 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A 9004-32-4 DMF submitted to regulatory agencies in the US is known as a USDMF. 9004-32-4 USDMF includes data on 9004-32-4's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The 9004-32-4 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of 9004-32-4 suppliers with USDMF on PharmaCompass.
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