Package 72162-1740-1

Brand: ciprofloxacin

Generic: ciprofloxacin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-1740-1
Digits Only 7216217401
Product NDC 72162-1740
Product ID 72162-1740_1c857923-9e16-49e7-9e35-cd0236601cc8
Description

100 TABLET, FILM COATED in 1 BOTTLE (72162-1740-1)

Marketing

Marketing Status
Marketed Since 2024-07-16
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": "1c857923-9e16-49e7-9e35-cd0236601cc8", "openfda": {"unii": ["4BA73M5E37"], "rxcui": ["197511"], "spl_set_id": ["d6bd5021-cf56-4c8a-b5a0-bbc8919740af"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (72162-1740-1)", "package_ndc": "72162-1740-1", "marketing_start_date": "20240716"}], "brand_name": "Ciprofloxacin", "product_id": "72162-1740_1c857923-9e16-49e7-9e35-cd0236601cc8", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "72162-1740", "generic_name": "Ciprofloxacin Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ciprofloxacin", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "250 mg/1"}], "application_number": "ANDA076126", "marketing_category": "ANDA", "marketing_start_date": "20091010", "listing_expiration_date": "20261231"}