Package 42708-192-14

Brand: ciprofloxacin

Generic: ciprofloxacin
NDC Package Sample

Package Facts

Identity

Package NDC 42708-192-14
Digits Only 4270819214
Product NDC 42708-192
Product ID 42708-192_4149d3b5-0be5-bc82-e063-6394a90aba00
Description

14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (42708-192-14)

Marketing

Marketing Status
Marketed Since 2025-10-17
Brand ciprofloxacin
Generic ciprofloxacin
Sample Package Yes

Linked Drug Pages (1)

ciprofloxacin ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4149d3b5-0be5-bc82-e063-6394a90aba00", "openfda": {"unii": ["4BA73M5E37"], "rxcui": ["309309"], "spl_set_id": ["4149d980-a6cd-c06d-e063-6394a90a47a1"], "manufacturer_name": ["QPharma, Inc."]}, "finished": true, "packaging": [{"sample": true, "description": "14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (42708-192-14)", "package_ndc": "42708-192-14", "marketing_start_date": "20251017"}], "brand_name": "ciprofloxacin", "product_id": "42708-192_4149d3b5-0be5-bc82-e063-6394a90aba00", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "42708-192", "generic_name": "ciprofloxacin", "labeler_name": "QPharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ciprofloxacin", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA076639", "marketing_category": "ANDA", "marketing_start_date": "20040910", "listing_expiration_date": "20261231"}