01 1ALP Pharm
02 1Abbott Laboratories
03 1Alembic Pharmaceuticals Limited
04 1Alfasigma
05 1Cyalume Specialty Products
06 1Dupont
07 2F. Hoffmann-La Roche
08 1Formosa Laboratories
09 1Harman Finochem
10 1PCA - Prodotti Chimicie Alimentari S.p.A
11 1Solara Active Pharma Sciences
12 1Symed Labs
13 1Taro Pharmaceutical Industries
14 5Blank
01 1MANUFACTURING AND CONTROL FOR PRODUCTION OF MEPROBAMATE
02 6MEPROBAMATE
03 1MEPROBAMATE (DRUG SUBSTANCE, NON-STERILE)
04 1MEPROBAMATE N.F.XII
05 1MEPROBAMATE POWDER-WITH TRACER
06 1MEPROBAMATE TABLETS
07 5MEPROBAMATE USP
08 1MEPROBAMATE-PRODUCED BY SHANSHI CORP IN TAIYUAN, PEOPLES' REPUB CHINA)
09 1MEPROSPAN 200MG S.R. CAPS
10 1MEPROSPAN 400MG S.R. CAPS.
01 1China
02 4India
03 2Italy
04 2Switzerland
05 1Taiwan
06 4U.S.A
07 5Blank
01 7Active
02 12Inactive
01 19Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 20420
Submission : 2007-03-28
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 482
Submission : 1962-04-26
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 18193
Submission : 2005-03-22
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 20465
Submission : 2007-04-23
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 20674
Submission : 2007-07-13
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 441
Submission : 1961-07-21
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 19680
Submission : 2006-08-07
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 19678
Submission : 2006-08-14
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 23284
Submission : 2009-12-09
Status : Active
Type : II
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 877
Submission : 1965-02-24
Status : Inactive
Type : II
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Corporate PDF
A Meprobamate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Meprobamate, including repackagers and relabelers. The FDA regulates Meprobamate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Meprobamate API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Meprobamate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Meprobamate supplier is an individual or a company that provides Meprobamate active pharmaceutical ingredient (API) or Meprobamate finished formulations upon request. The Meprobamate suppliers may include Meprobamate API manufacturers, exporters, distributors and traders.
click here to find a list of Meprobamate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Meprobamate DMF (Drug Master File) is a document detailing the whole manufacturing process of Meprobamate active pharmaceutical ingredient (API) in detail. Different forms of Meprobamate DMFs exist exist since differing nations have different regulations, such as Meprobamate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Meprobamate DMF submitted to regulatory agencies in the US is known as a USDMF. Meprobamate USDMF includes data on Meprobamate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Meprobamate USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Meprobamate suppliers with USDMF on PharmaCompass.
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