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Carisoprodol - 51525-5901-1 - (carisoprodol)

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Drug Information of Carisoprodol

Product NDC: 51525-5901
Proprietary Name: Carisoprodol
Non Proprietary Name: carisoprodol
Active Ingredient(s): 250    mg/1 & nbsp;   carisoprodol
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Carisoprodol

Product NDC: 51525-5901
Labeler Name: Wallace Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA011792
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20100701

Package Information of Carisoprodol

Package NDC: 51525-5901-1
Package Description: 100 TABLET in 1 BOTTLE (51525-5901-1)

NDC Information of Carisoprodol

NDC Code 51525-5901-1
Proprietary Name Carisoprodol
Package Description 100 TABLET in 1 BOTTLE (51525-5901-1)
Product NDC 51525-5901
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name carisoprodol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100701
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Wallace Pharmaceuticals Inc.
Substance Name CARISOPRODOL
Strength Number 250
Strength Unit mg/1
Pharmaceutical Classes Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC]

Complete Information of Carisoprodol


General Information