| NDC Code | 80425-0493-2 |
|---|
| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (80425-0493-2) |
|---|
| Product NDC | 80425-0493 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Ciprofloxacin Hydrochloride |
|---|
| Non-Proprietary Name | Ciprofloxacin Hydrochloride |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20250320 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA076593 |
|---|
| Manufacturer | Advanced Rx of Tennessee, LLC |
|---|
| Substance Name | CIPROFLOXACIN HYDROCHLORIDE |
|---|
| Strength | 500 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Cytochrome P450 1A2 Inhibitors [MoA], Fluoroquinolone Antibacterial [EPC], Fluoroquinolones [CS] |
|---|