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Carisoprodol - 52959-026-14 - (Carisoprodol)

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Drug Information of Carisoprodol

Product NDC: 52959-026
Proprietary Name: Carisoprodol
Non Proprietary Name: Carisoprodol
Active Ingredient(s): 350    mg/1 & nbsp;   Carisoprodol
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Carisoprodol

Product NDC: 52959-026
Labeler Name: H.J. Harkins Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040124
Marketing Category: ANDA
Start Marketing Date: 19960124

Package Information of Carisoprodol

Package NDC: 52959-026-14
Package Description: 14 TABLET in 1 BOTTLE, PLASTIC (52959-026-14)

NDC Information of Carisoprodol

NDC Code 52959-026-14
Proprietary Name Carisoprodol
Package Description 14 TABLET in 1 BOTTLE, PLASTIC (52959-026-14)
Product NDC 52959-026
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Carisoprodol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19960124
Marketing Category Name ANDA
Labeler Name H.J. Harkins Company, Inc.
Substance Name CARISOPRODOL
Strength Number 350
Strength Unit mg/1
Pharmaceutical Classes Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC]

Complete Information of Carisoprodol


General Information