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Carisoprodol - 62756-446-03 - (Carisoprodol)

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Drug Information of Carisoprodol

Product NDC: 62756-446
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: 62756-446
Labeler Name: Sun Pharmaceutical Industries Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040755
Marketing Category: ANDA
Start Marketing Date: 20070227

Package Information of Carisoprodol

Package NDC: 62756-446-03
Package Description: 100 TABLET in 1 BOTTLE (62756-446-03)

NDC Information of Carisoprodol

NDC Code 62756-446-03
Proprietary Name Carisoprodol
Package Description 100 TABLET in 1 BOTTLE (62756-446-03)
Product NDC 62756-446
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 Sun Pharmaceutical Industries Limited
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