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Meprobamate - 23155-129-10 - (Meprobamate)

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Drug Information of Meprobamate

Product NDC: 23155-129
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: 23155-129
Labeler Name: Heritage Pharmaceuticals Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090122
Marketing Category: ANDA
Start Marketing Date: 20090624

Package Information of Meprobamate

Package NDC: 23155-129-10
Package Description: 1000 TABLET in 1 BOTTLE (23155-129-10)

NDC Information of Meprobamate

NDC Code 23155-129-10
Proprietary Name Meprobamate
Package Description 1000 TABLET in 1 BOTTLE (23155-129-10)
Product NDC 23155-129
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Meprobamate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090624
Marketing Category Name ANDA
Labeler Name Heritage Pharmaceuticals Inc
Substance Name MEPROBAMATE
Strength Number 400
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Meprobamate


General Information