| NDC Code | 68084-069-01 |
|---|
| Package Description | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-069-01) > 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-069-11) |
|---|
| Product NDC | 68084-069 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Ciprofloxacin |
|---|
| Non-Proprietary Name | Ciprofloxacin Hydrochloride |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20040818 |
|---|
| End Marketing Date | 20211031 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA076794 |
|---|
| Manufacturer | American Health Packaging |
|---|
| Substance Name | CIPROFLOXACIN HYDROCHLORIDE |
|---|
| Strength | 250 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Quinolone Antimicrobial [EPC],Quinolones [CS] |
|---|