| NDC Code | 54868-4858-3 |
|---|
| Package Description | 15 TABLET, FILM COATED in 1 BOTTLE (54868-4858-3) |
|---|
| Product NDC | 54868-4858 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Ciprofloxacin |
|---|
| Non-Proprietary Name | Ciprofloxacin Hydrochloride |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20030912 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA076794 |
|---|
| Manufacturer | Physicians Total Care, Inc. |
|---|
| Substance Name | CIPROFLOXACIN HYDROCHLORIDE |
|---|
| Strength | 500 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient] |
|---|