SKELAXIN - 60793-136-05 - (metaxalone)

Alphabetical Index


Drug Information of SKELAXIN

Product NDC: 60793-136
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: 60793-136
Labeler Name: King Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA013217
Marketing Category: NDA
Start Marketing Date: 20020830

Package Information of SKELAXIN

Package NDC: 60793-136-05
Package Description: 500 TABLET in 1 BOTTLE (60793-136-05)

NDC Information of SKELAXIN

NDC Code 60793-136-05
Proprietary Name SKELAXIN
Package Description 500 TABLET in 1 BOTTLE (60793-136-05)
Product NDC 60793-136
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name metaxalone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20020830
Marketing Category Name NDA
Labeler Name King Pharmaceuticals, Inc.
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