Package 72789-065-20
Brand: ciprofloxacin
Generic: ciprofloxacin hydrochloridePackage Facts
Identity
Package NDC
72789-065-20
Digits Only
7278906520
Product NDC
72789-065
Description
20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-065-20)
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": "3403f8c6-f561-fe54-e063-6294a90a972b", "openfda": {"upc": ["0372789065205"], "unii": ["4BA73M5E37"], "rxcui": ["309309"], "spl_set_id": ["bb2edaca-6cf2-4100-83f5-8ce142f68e59"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-065-20)", "package_ndc": "72789-065-20", "marketing_start_date": "20200323"}], "brand_name": "Ciprofloxacin", "product_id": "72789-065_3403f8c6-f561-fe54-e063-6294a90a972b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "72789-065", "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": "ANDA076126", "marketing_category": "ANDA", "marketing_start_date": "20091010", "listing_expiration_date": "20261231"}