NDC Code | 0179-1982-14 |
Package Description | 14 TABLET in 1 BOTTLE (0179-1982-14) |
Product NDC | 0179-1982 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Ciprofloxacin Hydrochloride |
Non-Proprietary Name | Ciprofloxacin Hydrochloride |
Dosage Form | TABLET |
Usage | ORAL |
Start Marketing Date | 20110623 |
Marketing Category Name | ANDA |
Application Number | ANDA076089 |
Manufacturer | KAISER FOUNDATION HOSPITALS |
Substance Name | CIPROFLOXACIN HYDROCHLORIDE |
Strength | 500 |
Strength Unit | mg/1 |
Pharmacy Classes | Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient] |