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Carisoprodol - 55154-2072-0 - (Carisoprodol)

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Drug Information of Carisoprodol

Product NDC: 55154-2072
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: 55154-2072
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040245
Marketing Category: ANDA
Start Marketing Date: 20100115

Package Information of Carisoprodol

Package NDC: 55154-2072-0
Package Description: 10 BLISTER PACK in 1 BAG (55154-2072-0) > 1 TABLET in 1 BLISTER PACK

NDC Information of Carisoprodol

NDC Code 55154-2072-0
Proprietary Name Carisoprodol
Package Description 10 BLISTER PACK in 1 BAG (55154-2072-0) > 1 TABLET in 1 BLISTER PACK
Product NDC 55154-2072
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Carisoprodol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100115
Marketing Category Name ANDA
Labeler Name Cardinal Health
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