Package 67046-1528-3

Brand: ciprofloxacin

Generic: ciprofloxacin
NDC Package

Package Facts

Identity

Package NDC 67046-1528-3
Digits Only 6704615283
Product NDC 67046-1528
Product ID 67046-1528_2fff6ac3-455d-7df0-e063-6394a90a0672
Description

30 TABLET in 1 BLISTER PACK (67046-1528-3)

Marketing

Marketing Status
Marketed Since 2025-03-10
Brand ciprofloxacin
Generic ciprofloxacin
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": "2fff6ac3-455d-7df0-e063-6394a90a0672", "openfda": {"unii": ["4BA73M5E37"], "rxcui": ["197512"], "spl_set_id": ["2fff7a38-2c4e-d343-e063-6294a90aca3c"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (67046-1528-3)", "package_ndc": "67046-1528-3", "marketing_start_date": "20250310"}], "brand_name": "ciprofloxacin", "product_id": "67046-1528_2fff6ac3-455d-7df0-e063-6394a90a0672", "dosage_form": "TABLET", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "67046-1528", "generic_name": "ciprofloxacin", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ciprofloxacin", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA076639", "marketing_category": "ANDA", "marketing_start_date": "20250310", "listing_expiration_date": "20261231"}