Avelox - 55154-3516-0 - (moxifloxacin hydrochloride)

Alphabetical Index


Drug Information of Avelox

Product NDC: 55154-3516
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: 55154-3516
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021085
Marketing Category: NDA
Start Marketing Date: 20100302

Package Information of Avelox

Package NDC: 55154-3516-0
Package Description: 10 BLISTER PACK in 1 BAG (55154-3516-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Avelox

NDC Code 55154-3516-0
Proprietary Name Avelox
Package Description 10 BLISTER PACK in 1 BAG (55154-3516-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 55154-3516
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name moxifloxacin hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20100302
Marketing Category Name NDA
Labeler Name Cardinal Health
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