Package 43063-767-28
Brand: ciprofloxacin
Generic: ciprofloxacinPackage Facts
Identity
Package NDC
43063-767-28
Digits Only
4306376728
Product NDC
43063-767
Description
28 TABLET in 1 BOTTLE, PLASTIC (43063-767-28)
Marketing
Marketing Status
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": "36c1792e-ec69-ff9a-e063-6294a90a325b", "openfda": {"upc": ["0343063767283"], "unii": ["4BA73M5E37"], "rxcui": ["197512"], "spl_set_id": ["2491e6a9-3415-43b9-b31b-67331f52806a"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "28 TABLET in 1 BOTTLE, PLASTIC (43063-767-28)", "package_ndc": "43063-767-28", "marketing_start_date": "20170519"}], "brand_name": "ciprofloxacin", "product_id": "43063-767_36c1792e-ec69-ff9a-e063-6294a90a325b", "dosage_form": "TABLET", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "43063-767", "generic_name": "ciprofloxacin", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ciprofloxacin", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA076639", "marketing_category": "ANDA", "marketing_start_date": "20040910", "listing_expiration_date": "20261231"}