NDC Code | 70934-093-30 |
Package Description | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-093-30) |
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 | 20191014 |
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] |