Package 72789-368-14

Brand: ciprofloxacin

Generic: ciprofloxacin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72789-368-14
Digits Only 7278936814
Product NDC 72789-368
Description

14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-368-14)

Marketing

Marketing Status
Discontinued 2027-02-28
Brand ciprofloxacin
Generic ciprofloxacin hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3cf7faf2-4128-1b7b-e063-6394a90a27be", "openfda": {"upc": ["0372789368146"], "unii": ["4BA73M5E37"], "rxcui": ["309309"], "spl_set_id": ["d290a840-6c60-435f-a46b-6d9ef7b9e5f3"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-368-14)", "package_ndc": "72789-368-14", "marketing_end_date": "20270228", "marketing_start_date": "20231211"}], "brand_name": "Ciprofloxacin", "product_id": "72789-368_3cf7faf2-4128-1b7b-e063-6394a90a27be", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "72789-368", "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": "20270228", "marketing_start_date": "20070426"}