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Carisoprodol - 42254-068-30 - (Carisoprodol)

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Drug Information of Carisoprodol

Product NDC: 42254-068
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: 42254-068
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040755
Marketing Category: ANDA
Start Marketing Date: 20070227

Package Information of Carisoprodol

Package NDC: 42254-068-30
Package Description: 3 TABLET in 1 BOTTLE (42254-068-30)

NDC Information of Carisoprodol

NDC Code 42254-068-30
Proprietary Name Carisoprodol
Package Description 3 TABLET in 1 BOTTLE (42254-068-30)
Product NDC 42254-068
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Carisoprodol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20070227
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
Substance Name CARISOPRODOL
Strength Number 350
Strength Unit mg/1
Pharmaceutical Classes Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC]

Complete Information of Carisoprodol


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