Skelaxin - 21695-123-90 - (Metaxalone)

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Drug Information of Skelaxin

Product NDC: 21695-123
Proprietary Name: Skelaxin
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 Skelaxin

Product NDC: 21695-123
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA013217
Marketing Category: NDA
Start Marketing Date: 19620813

Package Information of Skelaxin

Package NDC: 21695-123-90
Package Description: 90 TABLET in 1 BOTTLE (21695-123-90)

NDC Information of Skelaxin

NDC Code 21695-123-90
Proprietary Name Skelaxin
Package Description 90 TABLET in 1 BOTTLE (21695-123-90)
Product NDC 21695-123
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metaxalone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19620813
Marketing Category Name NDA
Labeler Name Rebel Distributors Corp
Substance Name METAXALONE
Strength Number 800
Strength Unit mg/1
Pharmaceutical Classes Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC]

Complete Information of Skelaxin


General Information