Metaxalone - 68788-9896-0 - (Metaxalone)

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Drug Information of Metaxalone

Product NDC: 68788-9896
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: 68788-9896
Labeler Name: Preferred Pharmaceuticals, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA013217
Marketing Category: NDA
Start Marketing Date: 20120214

Package Information of Metaxalone

Package NDC: 68788-9896-0
Package Description: 100 TABLET in 1 BOTTLE (68788-9896-0)

NDC Information of Metaxalone

NDC Code 68788-9896-0
Proprietary Name Metaxalone
Package Description 100 TABLET in 1 BOTTLE (68788-9896-0)
Product NDC 68788-9896
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metaxalone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120214
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 Metaxalone


General Information