| NDC Code | 0378-2080-89 |
|---|
| Package Description | 50 TABLET in 1 BOTTLE, PLASTIC (0378-2080-89) |
|---|
| Product NDC | 0378-2080 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Moxifloxacin Hydrochloride |
|---|
| Non-Proprietary Name | Moxifloxacin Hydrochloride |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20150923 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA204635 |
|---|
| Manufacturer | Mylan Pharmaceuticals Inc. |
|---|
| Substance Name | MOXIFLOXACIN HYDROCHLORIDE |
|---|
| Strength | 400 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient] |
|---|