| NDC Code | 52959-734-20 |
|---|
| Package Description | 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (52959-734-20) |
|---|
| Product NDC | 52959-734 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Ciprofloxacin |
|---|
| Non-Proprietary Name | Ciprofloxacin Hydrochloride |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20040609 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA076794 |
|---|
| Manufacturer | H.J. Harkins Company, Inc. |
|---|
| Substance Name | CIPROFLOXACIN HYDROCHLORIDE |
|---|
| Strength | 750 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Quinolone Antimicrobial [EPC],Quinolones [CS] |
|---|