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Avelox
Avelox - 52125-525-02 - (moxifloxacin hydrochloride)
Drug Information of Avelox
| Product NDC: | 52125-525 |
| 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: | 52125-525 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021085 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20130524 |
Package Information of Avelox
| Package NDC: | 52125-525-02 |
| Package Description: | 30 TABLET, FILM COATED in 1 VIAL (52125-525-02) |
NDC Information of Avelox
| NDC Code | 52125-525-02 |
| Proprietary Name | Avelox |
| Package Description | 30 TABLET, FILM COATED in 1 VIAL (52125-525-02) |
| Product NDC | 52125-525 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | moxifloxacin hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20130524 |
| Marketing Category Name | NDA |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | MOXIFLOXACIN HYDROCHLORIDE |
| Strength Number | 400 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient] |
