Avelox - 67296-0154-1 - (moxifloxacin hydrochloride)

Alphabetical Index


Drug Information of Avelox

Product NDC: 67296-0154
Proprietary Name: Avelox
Non Proprietary Name: moxifloxacin hydrochloride
Active Ingredient(s): 400    mg/1 & nbsp;   moxifloxacin hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Avelox

Product NDC: 67296-0154
Labeler Name: RedPharm Drug Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021085
Marketing Category: NDA
Start Marketing Date: 20110225

Package Information of Avelox

Package NDC: 67296-0154-1
Package Description: 10 TABLET, FILM COATED in 1 BOTTLE (67296-0154-1)

NDC Information of Avelox

NDC Code 67296-0154-1
Proprietary Name Avelox
Package Description 10 TABLET, FILM COATED in 1 BOTTLE (67296-0154-1)
Product NDC 67296-0154
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name moxifloxacin hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110225
Marketing Category Name NDA
Labeler Name RedPharm Drug Inc.
Substance Name MOXIFLOXACIN HYDROCHLORIDE
Strength Number 400
Strength Unit mg/1
Pharmaceutical Classes Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient]

Complete Information of Avelox


General Information