Package 50090-7843-5

Brand: ciprofloxacin hydrochloride

Generic: ciprofloxacin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-7843-5
Digits Only 5009078435
Product NDC 50090-7843
Product ID 50090-7843_56da4ad6-dcd2-4df7-b174-e78c8e0127b6
Description

10 TABLET, FILM COATED in 1 BOTTLE (50090-7843-5)

Marketing

Marketing Status
Marketed Since 2025-12-30
Brand ciprofloxacin hydrochloride
Generic ciprofloxacin hydrochloride
Sample Package No

Linked Drug Pages (1)

Ciprofloxacin Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "56da4ad6-dcd2-4df7-b174-e78c8e0127b6", "openfda": {"unii": ["4BA73M5E37"], "rxcui": ["309309"], "spl_set_id": ["6d029ad2-a1e8-4c11-a5eb-e2257c6a0ddb"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (50090-7843-0)", "package_ndc": "50090-7843-0", "marketing_start_date": "20251230"}, {"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE (50090-7843-1)", "package_ndc": "50090-7843-1", "marketing_start_date": "20251230"}, {"sample": false, "description": "6 TABLET, FILM COATED in 1 BOTTLE (50090-7843-3)", "package_ndc": "50090-7843-3", "marketing_start_date": "20251230"}, {"sample": false, "description": "28 TABLET, FILM COATED in 1 BOTTLE (50090-7843-4)", "package_ndc": "50090-7843-4", "marketing_start_date": "20251230"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (50090-7843-5)", "package_ndc": "50090-7843-5", "marketing_start_date": "20251230"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-7843-7)", "package_ndc": "50090-7843-7", "marketing_start_date": "20251230"}, {"sample": false, "description": "1 TABLET, FILM COATED in 1 BOTTLE (50090-7843-8)", "package_ndc": "50090-7843-8", "marketing_start_date": "20251230"}], "brand_name": "Ciprofloxacin Hydrochloride", "product_id": "50090-7843_56da4ad6-dcd2-4df7-b174-e78c8e0127b6", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "50090-7843", "generic_name": "Ciprofloxacin Hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ciprofloxacin Hydrochloride", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA076593", "marketing_category": "ANDA", "marketing_start_date": "20240523", "listing_expiration_date": "20271231"}