| NDC Code | 72205-001-31 |
|---|
| Package Description | 50 BLISTER PACK in 1 CARTON (72205-001-31) > 10 TABLET, FILM COATED in 1 BLISTER PACK (72205-001-11) |
|---|
| Product NDC | 72205-001 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Moxifloxacin Hydrochloride Tablets, 400 Mg |
|---|
| Non-Proprietary Name | Moxifloxacin Hydrochloride Tablets, 400 Mg |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20180721 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA208682 |
|---|
| Manufacturer | Novadoz Pharmaceuticals LLC |
|---|
| Substance Name | MOXIFLOXACIN HYDROCHLORIDE MONOHYDRATE |
|---|
| Strength | 400 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Quinolone Antimicrobial [EPC], Quinolones [CS] |
|---|