| NDC Code | 55111-423-78 |
|---|
| Package Description | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOX, UNIT-DOSE (55111-423-78) |
|---|
| Product NDC | 55111-423 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Ciprofloxacin |
|---|
| Non-Proprietary Name | Ciprofloxacin Hydrochloride |
|---|
| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20071031 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA077701 |
|---|
| Manufacturer | Dr. Reddy's Laboratories Limited |
|---|
| Substance Name | CIPROFLOXACIN HYDROCHLORIDE; CIPROFLOXACIN |
|---|
| Strength | 574.9; 425.2 |
|---|
| Strength Unit | mg/1; mg/1 |
|---|
| Pharmacy Classes | Quinolone Antimicrobial [EPC],Quinolones [CS],Quinolone Antimicrobial [EPC],Quinolones [CS] |
|---|