| NDC Code | 68084-722-65 |
|---|
| Package Description | 50 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-722-65) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-722-11) |
|---|
| Product NDC | 68084-722 |
|---|
| 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 | 20140319 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA202632 |
|---|
| Manufacturer | American Health Packaging |
|---|
| Substance Name | MOXIFLOXACIN HYDROCHLORIDE |
|---|
| Strength | 400 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Fluoroquinolone Antibacterial [EPC], Fluoroquinolones [CS] |
|---|