Metaxalone - 64720-321-50 - (Metaxalone)

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Drug Information of Metaxalone

Product NDC: 64720-321
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: 64720-321
Labeler Name: CorePharma, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA013217
Marketing Category: NDA
Start Marketing Date: 20071101

Package Information of Metaxalone

Package NDC: 64720-321-50
Package Description: 500 TABLET in 1 BOTTLE (64720-321-50)

NDC Information of Metaxalone

NDC Code 64720-321-50
Proprietary Name Metaxalone
Package Description 500 TABLET in 1 BOTTLE (64720-321-50)
Product NDC 64720-321
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metaxalone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20071101
Marketing Category Name NDA
Labeler Name CorePharma, LLC
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