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Carisoprodol - 49349-830-02 - (Carisoprodol)

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Drug Information of Carisoprodol

Product NDC: 49349-830
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: 49349-830
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040245
Marketing Category: ANDA
Start Marketing Date: 20130509

Package Information of Carisoprodol

Package NDC: 49349-830-02
Package Description: 30 TABLET in 1 BLISTER PACK (49349-830-02)

NDC Information of Carisoprodol

NDC Code 49349-830-02
Proprietary Name Carisoprodol
Package Description 30 TABLET in 1 BLISTER PACK (49349-830-02)
Product NDC 49349-830
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Carisoprodol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130509
Marketing Category Name ANDA
Labeler Name REMEDYREPACK 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


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