| NDC Code | 54868-0990-5 |
|---|
| Package Description | 6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-0990-5) |
|---|
| Product NDC | 54868-0990 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Cipro |
|---|
| Non-Proprietary Name | Ciprofloxacin Hydrochloride |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 19950207 |
|---|
| Marketing Category Name | NDA |
|---|
| Application Number | NDA019537 |
|---|
| Manufacturer | Physicians Total Care, Inc. |
|---|
| Substance Name | CIPROFLOXACIN HYDROCHLORIDE |
|---|
| Strength | 250 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient] |
|---|