Package 83008-078-20

Brand: ciprofloxacin

Generic: ciprofolxacin
NDC Package

Package Facts

Identity

Package NDC 83008-078-20
Digits Only 8300807820
Product NDC 83008-078
Product ID 83008-078_d6e43461-8fb9-44e4-998b-b501bbabf58b
Description

20 TABLET in 1 BOTTLE (83008-078-20)

Marketing

Marketing Status
Discontinued 2026-08-31
Brand ciprofloxacin
Generic ciprofolxacin
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": "d6e43461-8fb9-44e4-998b-b501bbabf58b", "openfda": {"unii": ["4BA73M5E37"], "rxcui": ["309309"], "spl_set_id": ["a0eda476-1625-4e9e-bb76-4f1cf05562f0"], "manufacturer_name": ["Quality Care Products, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE (83008-078-20)", "package_ndc": "83008-078-20", "marketing_end_date": "20260831", "marketing_start_date": "20240821"}], "brand_name": "Ciprofloxacin", "product_id": "83008-078_d6e43461-8fb9-44e4-998b-b501bbabf58b", "dosage_form": "TABLET", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "83008-078", "generic_name": "Ciprofolxacin", "labeler_name": "Quality Care Products, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ciprofloxacin", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA208921", "marketing_category": "ANDA", "marketing_end_date": "20260831", "marketing_start_date": "20240821"}