| NDC Code | 10370-107-10 |
|---|
| Package Description | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (10370-107-10) |
|---|
| Product NDC | 10370-107 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Ciprofloxacin |
|---|
| Proprietary Name Suffix | Extended-release |
|---|
| Non-Proprietary Name | Ciprofloxacin |
|---|
| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20110805 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA078166 |
|---|
| Manufacturer | Par Pharmaceutical, Inc. |
|---|
| Substance Name | CIPROFLOXACIN HYDROCHLORIDE; CIPROFLOXACIN |
|---|
| Strength | 212.6; 287.5 |
|---|
| Strength Unit | mg/1; mg/1 |
|---|
| Pharmacy Classes | Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient],Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient] |
|---|