| NDC Code | 60429-893-30 |
|---|
| Package Description | 30 TABLET in 1 BOTTLE (60429-893-30) |
|---|
| Product NDC | 60429-893 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Moxifloxacin Hydrochloride |
|---|
| Non-Proprietary Name | Moxifloxacin Hydrochloride |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20160114 |
|---|
| End Marketing Date | 20250731 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA205348 |
|---|
| Manufacturer | Golden State Medical Supply, Inc. |
|---|
| Substance Name | MOXIFLOXACIN HYDROCHLORIDE |
|---|
| Strength | 400 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Fluoroquinolone Antibacterial [EPC], Fluoroquinolones [CS] |
|---|