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