Package 72789-302-14
Brand: ciprofloxacin
Generic: ciprofloxacin hydrochloridePackage Facts
Identity
Package NDC
72789-302-14
Digits Only
7278930214
Product NDC
72789-302
Description
14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-302-14)
Marketing
Marketing Status
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": "3cf6c52b-1263-b5f5-e063-6394a90a9ef7", "openfda": {"upc": ["0372789302065"], "unii": ["4BA73M5E37"], "rxcui": ["197511"], "spl_set_id": ["ef07c7f4-4ccf-44f6-aee9-add6d3b0b9d2"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-302-06)", "package_ndc": "72789-302-06", "marketing_end_date": "20270131", "marketing_start_date": "20230327"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-302-10)", "package_ndc": "72789-302-10", "marketing_end_date": "20270131", "marketing_start_date": "20230301"}, {"sample": false, "description": "12 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-302-12)", "package_ndc": "72789-302-12", "marketing_end_date": "20270131", "marketing_start_date": "20230410"}, {"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-302-14)", "package_ndc": "72789-302-14", "marketing_end_date": "20270131", "marketing_start_date": "20230516"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-302-20)", "package_ndc": "72789-302-20", "marketing_end_date": "20270131", "marketing_start_date": "20230814"}], "brand_name": "Ciprofloxacin", "product_id": "72789-302_3cf6c52b-1263-b5f5-e063-6394a90a9ef7", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "72789-302", "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": "250 mg/1"}], "application_number": "ANDA077859", "marketing_category": "ANDA", "marketing_end_date": "20270131", "marketing_start_date": "20070426"}