Package 72789-124-01

Brand: ciprofloxacin

Generic: ciprofloxacin
NDC Package

Package Facts

Identity

Package NDC 72789-124-01
Digits Only 7278912401
Product NDC 72789-124
Description

100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-124-01)

Marketing

Marketing Status
Marketed Since 2020-10-07
Brand ciprofloxacin
Generic ciprofloxacin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2d675959-9721-1fd0-e063-6294a90aad29", "openfda": {"upc": ["0372789125503", "0372789124018"], "unii": ["4BA73M5E37"], "rxcui": ["197511", "197512"], "spl_set_id": ["5723eaf9-8659-4730-b792-4e4c33690ccb"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-124-01)", "package_ndc": "72789-124-01", "marketing_start_date": "20201007"}], "brand_name": "Ciprofloxacin", "product_id": "72789-124_2d675959-9721-1fd0-e063-6294a90aad29", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "72789-124", "generic_name": "Ciprofloxacin", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ciprofloxacin", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "250 mg/1"}], "application_number": "ANDA076558", "marketing_category": "ANDA", "marketing_start_date": "20040609", "listing_expiration_date": "20261231"}