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Avelox ABC Pack - 16590-881-05 - (MOXIFLOXACIN HYDROCHLORIDE)

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Drug Information of Avelox ABC Pack

Product NDC: 16590-881
Proprietary Name: Avelox ABC Pack
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 ABC Pack

Product NDC: 16590-881
Labeler Name: Stat Rx USA
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021085
Marketing Category: NDA
Start Marketing Date: 19991210

Package Information of Avelox ABC Pack

Package NDC: 16590-881-05
Package Description: 5 TABLET, FILM COATED in 1 BOX, UNIT-DOSE (16590-881-05)

NDC Information of Avelox ABC Pack

NDC Code 16590-881-05
Proprietary Name Avelox ABC Pack
Package Description 5 TABLET, FILM COATED in 1 BOX, UNIT-DOSE (16590-881-05)
Product NDC 16590-881
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name MOXIFLOXACIN HYDROCHLORIDE
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19991210
Marketing Category Name NDA
Labeler Name Stat Rx USA
Substance Name MOXIFLOXACIN HYDROCHLORIDE
Strength Number 400
Strength Unit mg/1
Pharmaceutical Classes Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient]

Complete Information of Avelox ABC Pack


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