NDC Code | 68084-071-01 |
Package Description | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-071-01) > 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-071-11) |
Product NDC | 68084-071 |
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 |
Marketing Category Name | ANDA |
Application Number | ANDA076794 |
Manufacturer | American Health Packaging |
Substance Name | CIPROFLOXACIN HYDROCHLORIDE |
Strength | 750 |
Strength Unit | mg/1 |
Pharmacy Classes | Quinolone Antimicrobial [EPC], Quinolones [CS] |