| NDC Code | 65862-603-55 |
|---|
| Package Description | 50 BLISTER PACK in 1 BOX, UNIT-DOSE (65862-603-55) / 1 TABLET, FILM COATED in 1 BLISTER PACK (65862-603-10) |
|---|
| Product NDC | 65862-603 |
|---|
| 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 | 20140304 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA202632 |
|---|
| Manufacturer | Aurobindo Pharma Limited |
|---|
| Substance Name | MOXIFLOXACIN HYDROCHLORIDE |
|---|
| Strength | 400 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Fluoroquinolone Antibacterial [EPC], Fluoroquinolones [CS] |
|---|