Package 82982-050-14

Brand: ciprofloxacin

Generic: ciprofloxacin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 82982-050-14
Digits Only 8298205014
Product NDC 82982-050
Product ID 82982-050_198d06e8-115c-8ac3-e063-6394a90a978e
Description

14 TABLET, FILM COATED in 1 BOTTLE (82982-050-14)

Marketing

Marketing Status
Discontinued 2026-07-31
Brand ciprofloxacin
Generic ciprofloxacin hydrochloride
Sample Package No

Linked Drug Pages (1)

Ciprofloxacin ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "198d06e8-115c-8ac3-e063-6394a90a978e", "openfda": {"upc": ["0382982050144", "0382982050205"], "unii": ["4BA73M5E37"], "rxcui": ["309309"], "spl_set_id": ["f2937a87-2e10-3728-e053-2a95a90a9eb9"], "manufacturer_name": ["Pharmasource Meds, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE (82982-050-14)", "package_ndc": "82982-050-14", "marketing_end_date": "20260731", "marketing_start_date": "20230123"}], "brand_name": "Ciprofloxacin", "product_id": "82982-050_198d06e8-115c-8ac3-e063-6394a90a978e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "82982-050", "generic_name": "Ciprofloxacin Hydrochloride", "labeler_name": "Pharmasource Meds, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ciprofloxacin", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA077859", "marketing_category": "ANDA", "marketing_end_date": "20260731", "marketing_start_date": "20230123"}