NDC Code | 72789-080-10 |
Package Description | 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-080-10) |
Product NDC | 72789-080 |
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 | PD-Rx Pharmaceuticals, Inc. |
Substance Name | MOXIFLOXACIN HYDROCHLORIDE MONOHYDRATE |
Strength | 400 |
Strength Unit | mg/1 |
Pharmacy Classes | Fluoroquinolone Antibacterial [EPC], Fluoroquinolones [CS] |