Avelox - 49999-455-05 - (moxifloxacin hydrochloride)

Alphabetical Index


Drug Information of Avelox

Product NDC: 49999-455
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, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Avelox

Product NDC: 49999-455
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021085
Marketing Category: NDA
Start Marketing Date: 20111207

Package Information of Avelox

Package NDC: 49999-455-05
Package Description: 5 TABLET, COATED in 1 BOTTLE (49999-455-05)

NDC Information of Avelox

NDC Code 49999-455-05
Proprietary Name Avelox
Package Description 5 TABLET, COATED in 1 BOTTLE (49999-455-05)
Product NDC 49999-455
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name moxifloxacin hydrochloride
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20111207
Marketing Category Name NDA
Labeler Name Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
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