Skelaxin - 68788-0881-1 - (Metaxalone)

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Drug Information of Skelaxin

Product NDC: 68788-0881
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: 68788-0881
Labeler Name: Preferred Pharmaceuticals, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA013217
Marketing Category: NDA
Start Marketing Date: 20030130

Package Information of Skelaxin

Package NDC: 68788-0881-1
Package Description: 120 TABLET in 1 BOTTLE (68788-0881-1)

NDC Information of Skelaxin

NDC Code 68788-0881-1
Proprietary Name Skelaxin
Package Description 120 TABLET in 1 BOTTLE (68788-0881-1)
Product NDC 68788-0881
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metaxalone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20030130
Marketing Category Name NDA
Labeler Name Preferred 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