| NDC Code | 67296-0142-1 |
|---|
| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (67296-0142-1) / 5 mL in 1 BOTTLE, PLASTIC |
|---|
| Product NDC | 67296-0142 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Ciprofloxacin Hydrochloride |
|---|
| Non-Proprietary Name | Ciprofloxacin Hydrochloride |
|---|
| Dosage Form | SOLUTION/ DROPS |
|---|
| Usage | OPHTHALMIC |
|---|
| Start Marketing Date | 20040507 |
|---|
| Marketing Category Name | NDA AUTHORIZED GENERIC |
|---|
| Application Number | NDA019992 |
|---|
| Manufacturer | Redpharm Drug |
|---|
| Substance Name | CIPROFLOXACIN HYDROCHLORIDE |
|---|
| Strength | 3 |
|---|
| Strength Unit | mg/mL |
|---|
| Pharmacy Classes | Cytochrome P450 1A2 Inhibitors [MoA], Fluoroquinolone Antibacterial [EPC], Fluoroquinolones [CS] |
|---|