Package 68071-3351-3

Brand: ciprofloxacin hydrochloride

Generic: ciprofloxacin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-3351-3
Digits Only 6807133513
Product NDC 68071-3351
Product ID 68071-3351_1ce8f03a-6915-908c-e063-6394a90a270c
Description

10 mL in 1 BOX (68071-3351-3)

Marketing

Marketing Status
Marketed Since 2017-07-20
Brand ciprofloxacin hydrochloride
Generic ciprofloxacin hydrochloride
Sample Package No

Linked Drug Pages (1)

Ciprofloxacin Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["OPHTHALMIC"], "spl_id": "1ce8f03a-6915-908c-e063-6394a90a270c", "openfda": {"unii": ["4BA73M5E37"], "rxcui": ["309307"], "spl_set_id": ["54c73290-bd89-3453-e054-00144ff88e88"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "10 mL in 1 BOX (68071-3351-3)", "package_ndc": "68071-3351-3", "marketing_start_date": "20170720"}], "brand_name": "Ciprofloxacin Hydrochloride", "product_id": "68071-3351_1ce8f03a-6915-908c-e063-6394a90a270c", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "68071-3351", "generic_name": "Ciprofloxacin Hydrochloride", "labeler_name": "NuCare Pharmaceuticals,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": "20040507", "listing_expiration_date": "20261231"}