Package 72789-520-06

Brand: ciprofloxacin

Generic: ciprofloxacin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72789-520-06
Digits Only 7278952006
Product NDC 72789-520
Product ID 72789-520_3c54f52e-9a55-3cd7-e063-6294a90a5bad
Description

6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-520-06)

Marketing

Marketing Status
Discontinued 2028-02-29
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": "3c54f52e-9a55-3cd7-e063-6294a90a5bad", "openfda": {"unii": ["4BA73M5E37"], "rxcui": ["309309"], "spl_set_id": ["3c611c8c-deed-4904-93f7-f75a2147fbf7"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-520-06)", "package_ndc": "72789-520-06", "marketing_end_date": "20280229", "marketing_start_date": "20250814"}], "brand_name": "Ciprofloxacin", "product_id": "72789-520_3c54f52e-9a55-3cd7-e063-6294a90a5bad", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "72789-520", "generic_name": "Ciprofloxacin Hydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ciprofloxacin", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA077859", "marketing_category": "ANDA", "marketing_end_date": "20280229", "marketing_start_date": "20240209"}