| NDC Code | 70518-4458-0 |
|---|
| Package Description | 7 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4458-0) |
|---|
| Product NDC | 70518-4458 |
|---|
| 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 | 20250827 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA202632 |
|---|
| Manufacturer | REMEDYREPACK INC. |
|---|
| Substance Name | MOXIFLOXACIN HYDROCHLORIDE |
|---|
| Strength | 400 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Fluoroquinolone Antibacterial [EPC], Fluoroquinolones [CS] |
|---|