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Meprobamate - 55111-641-01 - (Meprobamate)

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Drug Information of Meprobamate

Product NDC: 55111-641
Proprietary Name: Meprobamate
Non Proprietary Name: Meprobamate
Active Ingredient(s): 400    mg/1 & nbsp;   Meprobamate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Meprobamate

Product NDC: 55111-641
Labeler Name: Dr.Reddy's Laboratories Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040797
Marketing Category: ANDA
Start Marketing Date: 20080103

Package Information of Meprobamate

Package NDC: 55111-641-01
Package Description: 100 TABLET in 1 BOTTLE (55111-641-01)

NDC Information of Meprobamate

NDC Code 55111-641-01
Proprietary Name Meprobamate
Package Description 100 TABLET in 1 BOTTLE (55111-641-01)
Product NDC 55111-641
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Meprobamate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20080103
Marketing Category Name ANDA
Labeler Name Dr.Reddy's Laboratories Limited
Substance Name MEPROBAMATE
Strength Number 400
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Meprobamate


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