Package 70518-1170-0

Brand: ciprofloxacin hydrochloride

Generic: ciprofloxacin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-1170-0
Digits Only 7051811700
Product NDC 70518-1170
Description

1 BOTTLE, PLASTIC in 1 CARTON (70518-1170-0) / 5 mL in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Marketed Since 2018-05-15
Brand ciprofloxacin hydrochloride
Generic ciprofloxacin hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "36e8be23-f959-0d00-e063-6294a90ae770", "openfda": {"unii": ["4BA73M5E37"], "rxcui": ["309307"], "spl_set_id": ["a2cec2cc-729b-4baa-8df1-c3f70847a483"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (70518-1170-0)  / 5 mL in 1 BOTTLE, PLASTIC", "package_ndc": "70518-1170-0", "marketing_start_date": "20180515"}], "brand_name": "Ciprofloxacin Hydrochloride", "product_id": "70518-1170_36e8be23-f959-0d00-e063-6294a90ae770", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "70518-1170", "generic_name": "Ciprofloxacin Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ciprofloxacin Hydrochloride", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "3 mg/mL"}], "application_number": "NDA019992", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20180515", "listing_expiration_date": "20261231"}