NDC Code | 70934-093-06 |
Package Description | 6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-093-06) |
Product NDC | 70934-093 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Ciprofloxacin |
Non-Proprietary Name | Ciprofloxacin Hydrochloride |
Dosage Form | TABLET, FILM COATED |
Usage | ORAL |
Start Marketing Date | 20070426 |
End Marketing Date | 20250131 |
Marketing Category Name | ANDA |
Application Number | ANDA077859 |
Manufacturer | Denton Pharma, Inc. DBA Northwind Pharmaceuticals |
Substance Name | CIPROFLOXACIN HYDROCHLORIDE |
Strength | 500 |
Strength Unit | mg/1 |
Pharmacy Classes | Quinolone Antimicrobial [EPC], Quinolones [CS] |