Metaxalone - 54868-6102-0 - (Metaxalone)

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Drug Information of Metaxalone

Product NDC: 54868-6102
Proprietary Name: Metaxalone
Non Proprietary Name: Metaxalone
Active Ingredient(s): 800    mg/1 & nbsp;   Metaxalone
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Metaxalone

Product NDC: 54868-6102
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040445
Marketing Category: ANDA
Start Marketing Date: 20100407

Package Information of Metaxalone

Package NDC: 54868-6102-0
Package Description: 10 TABLET in 1 BOTTLE (54868-6102-0)

NDC Information of Metaxalone

NDC Code 54868-6102-0
Proprietary Name Metaxalone
Package Description 10 TABLET in 1 BOTTLE (54868-6102-0)
Product NDC 54868-6102
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metaxalone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100407
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name METAXALONE
Strength Number 800
Strength Unit mg/1
Pharmaceutical Classes Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC]

Complete Information of Metaxalone


General Information