Package 72789-330-28

Brand: ciprofloxacin

Generic: ciprofloxacin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72789-330-28
Digits Only 7278933028
Product NDC 72789-330
Description

28 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-330-28)

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": "3cf6f764-1e6f-6036-e063-6294a90aa8e9", "openfda": {"upc": ["0372789330204"], "unii": ["4BA73M5E37"], "rxcui": ["309309"], "spl_set_id": ["a2ffa81a-86c5-40b9-8fa0-c889801ef479"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-330-06)", "package_ndc": "72789-330-06", "marketing_end_date": "20270228", "marketing_start_date": "20230830"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-330-10)", "package_ndc": "72789-330-10", "marketing_end_date": "20270228", "marketing_start_date": "20230907"}, {"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-330-14)", "package_ndc": "72789-330-14", "marketing_end_date": "20270228", "marketing_start_date": "20230814"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-330-20)", "package_ndc": "72789-330-20", "marketing_end_date": "20270228", "marketing_start_date": "20230706"}, {"sample": false, "description": "28 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-330-28)", "package_ndc": "72789-330-28", "marketing_end_date": "20270228", "marketing_start_date": "20230807"}], "brand_name": "Ciprofloxacin", "product_id": "72789-330_3cf6f764-1e6f-6036-e063-6294a90aa8e9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "72789-330", "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"}