| NDC Code | 43063-585-05 |
|---|
| Package Description | 5 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-585-05) |
|---|
| Product NDC | 43063-585 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Moxifloxacin Hydrochloride |
|---|
| Non-Proprietary Name | Moxifloxacin Hydrochloride |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20140129 |
|---|
| Marketing Category Name | NDA AUTHORIZED GENERIC |
|---|
| Application Number | NDA021085 |
|---|
| Manufacturer | PD-Rx Pharmaceuticals, Inc. |
|---|
| Substance Name | MOXIFLOXACIN HYDROCHLORIDE |
|---|
| Strength | 400 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Quinolone Antimicrobial [EPC],Quinolones [CS] |
|---|