Package 68071-3737-6

Brand: ciprofloxacin

Generic: ciprofolxacin
NDC Package

Package Facts

Identity

Package NDC 68071-3737-6
Digits Only 6807137376
Product NDC 68071-3737
Description

6 TABLET in 1 BOTTLE (68071-3737-6)

Marketing

Marketing Status
Marketed Since 2025-06-04
Brand ciprofloxacin
Generic ciprofolxacin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "36c17958-0221-9987-e063-6294a90ac4f7", "openfda": {"upc": ["0368071373721"], "unii": ["4BA73M5E37"], "rxcui": ["309309"], "spl_set_id": ["288ea7b2-ecf2-e8e0-e063-6294a90a306a"], "manufacturer_name": ["NuCare Pharmaceutical, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "2 TABLET in 1 BOTTLE (68071-3737-2)", "package_ndc": "68071-3737-2", "marketing_start_date": "20241205"}, {"sample": false, "description": "6 TABLET in 1 BOTTLE (68071-3737-6)", "package_ndc": "68071-3737-6", "marketing_start_date": "20250604"}], "brand_name": "Ciprofloxacin", "product_id": "68071-3737_36c17958-0221-9987-e063-6294a90ac4f7", "dosage_form": "TABLET", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "68071-3737", "generic_name": "Ciprofolxacin", "labeler_name": "NuCare Pharmaceutical, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ciprofloxacin", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA208921", "marketing_category": "ANDA", "marketing_start_date": "20231001", "listing_expiration_date": "20261231"}