Package 68071-3901-1

Brand: ciprofloxacin

Generic: ciprofolxacin
NDC Package

Package Facts

Identity

Package NDC 68071-3901-1
Digits Only 6807139011
Product NDC 68071-3901
Product ID 68071-3901_4120667b-faff-54da-e063-6394a90ace2a
Description

100 TABLET in 1 BOTTLE (68071-3901-1)

Marketing

Marketing Status
Marketed Since 2025-10-14
Brand ciprofloxacin
Generic ciprofolxacin
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": "4120667b-faff-54da-e063-6394a90ace2a", "openfda": {"upc": ["0368071390117"], "unii": ["4BA73M5E37"], "rxcui": ["197511"], "spl_set_id": ["41206a0f-7a5b-6a12-e063-6394a90a58b1"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68071-3901-1)", "package_ndc": "68071-3901-1", "marketing_start_date": "20251014"}], "brand_name": "Ciprofloxacin", "product_id": "68071-3901_4120667b-faff-54da-e063-6394a90ace2a", "dosage_form": "TABLET", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "68071-3901", "generic_name": "Ciprofolxacin", "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": "ANDA208921", "marketing_category": "ANDA", "marketing_start_date": "20231001", "listing_expiration_date": "20261231"}