Package 67046-1537-3

Brand: ciprofloxacin

Generic: ciprofolxacin
NDC Package

Package Facts

Identity

Package NDC 67046-1537-3
Digits Only 6704615373
Product NDC 67046-1537
Product ID 67046-1537_3134401f-7258-6c37-e063-6294a90a8fa9
Description

30 TABLET in 1 BLISTER PACK (67046-1537-3)

Marketing

Marketing Status
Marketed Since 2025-03-25
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": "3134401f-7258-6c37-e063-6294a90a8fa9", "openfda": {"unii": ["4BA73M5E37"], "rxcui": ["309309"], "spl_set_id": ["3134401f-72a3-6c37-e063-6294a90a8fa9"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (67046-1537-3)", "package_ndc": "67046-1537-3", "marketing_start_date": "20250325"}], "brand_name": "Ciprofloxacin", "product_id": "67046-1537_3134401f-7258-6c37-e063-6294a90a8fa9", "dosage_form": "TABLET", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "67046-1537", "generic_name": "Ciprofolxacin", "labeler_name": "Coupler LLC", "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": "20250325", "listing_expiration_date": "20261231"}