Package 68071-3876-2

Brand: ciprofloxacin

Generic: ciprofloxacin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-3876-2
Digits Only 6807138762
Product NDC 68071-3876
Product ID 68071-3876_3ab54634-3869-de53-e063-6394a90aabe9
Description

2 TABLET, FILM COATED in 1 BOTTLE (68071-3876-2)

Marketing

Marketing Status
Marketed Since 2025-07-24
Brand ciprofloxacin
Generic ciprofloxacin hydrochloride
Sample Package No

Linked Drug Pages (1)

Ciprofloxacin ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3ab54634-3869-de53-e063-6394a90aabe9", "openfda": {"upc": ["0368071387629"], "unii": ["4BA73M5E37"], "rxcui": ["197511"], "spl_set_id": ["3ab54ca0-1b12-d0f5-e063-6394a90a9575"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "2 TABLET, FILM COATED in 1 BOTTLE (68071-3876-2)", "package_ndc": "68071-3876-2", "marketing_start_date": "20250724"}], "brand_name": "Ciprofloxacin", "product_id": "68071-3876_3ab54634-3869-de53-e063-6394a90aabe9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "68071-3876", "generic_name": "Ciprofloxacin Hydrochloride", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ciprofloxacin", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "250 mg/1"}], "application_number": "ANDA077859", "marketing_category": "ANDA", "marketing_start_date": "20070426", "listing_expiration_date": "20261231"}