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carisoprodol - 65862-158-99 - (carisoprodol)

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Drug Information of carisoprodol

Product NDC: 65862-158
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: 65862-158
Labeler Name: Aurobindo Pharma Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040792
Marketing Category: ANDA
Start Marketing Date: 20090806

Package Information of carisoprodol

Package NDC: 65862-158-99
Package Description: 1000 TABLET in 1 BOTTLE (65862-158-99)

NDC Information of carisoprodol

NDC Code 65862-158-99
Proprietary Name carisoprodol
Package Description 1000 TABLET in 1 BOTTLE (65862-158-99)
Product NDC 65862-158
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name carisoprodol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090806
Marketing Category Name ANDA
Labeler Name Aurobindo Pharma 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


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