Metaxalone - 43063-239-15 - (Metaxalone)

Alphabetical Index


Drug Information of Metaxalone

Product NDC: 43063-239
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: 43063-239
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA013217
Marketing Category: NDA
Start Marketing Date: 20071101

Package Information of Metaxalone

Package NDC: 43063-239-15
Package Description: 15 TABLET in 1 BOTTLE, PLASTIC (43063-239-15)

NDC Information of Metaxalone

NDC Code 43063-239-15
Proprietary Name Metaxalone
Package Description 15 TABLET in 1 BOTTLE, PLASTIC (43063-239-15)
Product NDC 43063-239
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 PD-Rx 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