NDC Code | 13913-001-03 |
Package Description | 1 BLISTER PACK in 1 CARTON (13913-001-03) > 3 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK |
Product NDC | 13913-001 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Proquin |
Proprietary Name Suffix | Xr |
Non-Proprietary Name | Ciprofloxacin Hydrochloride |
Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
Usage | ORAL |
Start Marketing Date | 20051001 |
Marketing Category Name | NDA |
Application Number | NDA021744 |
Manufacturer | Depomed, Inc. |
Substance Name | CIPROFLOXACIN HYDROCHLORIDE |
Strength | 500 |
Strength Unit | mg/1 |
Pharmacy Classes | Quinolone Antimicrobial [EPC],Quinolones [CS] |