Package 16252-515-01

Brand: ciprofloxacin

Generic: ciprofloxacin
NDC Package

Package Facts

Identity

Package NDC 16252-515-01
Digits Only 1625251501
Product NDC 16252-515
Description

100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (16252-515-01)

Marketing

Marketing Status
Discontinued 2027-08-31
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": "102b18ad-5814-4bda-9b89-2991af2480e1", "openfda": {"upc": ["0316252515019"], "unii": ["4BA73M5E37"], "rxcui": ["197511", "197512", "309309"], "spl_set_id": ["3e4402d4-e0d3-9846-3e81-ed46f34137fe"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (16252-515-01)", "package_ndc": "16252-515-01", "marketing_end_date": "20270831", "marketing_start_date": "20061101"}], "brand_name": "Ciprofloxacin", "product_id": "16252-515_102b18ad-5814-4bda-9b89-2991af2480e1", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "16252-515", "generic_name": "Ciprofloxacin", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ciprofloxacin", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA076794", "marketing_category": "ANDA", "marketing_end_date": "20270831", "marketing_start_date": "20061101"}