Package 50090-7848-1

Brand: ciprofloxacin hydrochloride

Generic: ciprofloxacin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-7848-1
Digits Only 5009078481
Product NDC 50090-7848
Description

14 TABLET, FILM COATED in 1 BOTTLE (50090-7848-1)

Marketing

Marketing Status
Marketed Since 2026-01-05
Brand ciprofloxacin hydrochloride
Generic ciprofloxacin hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0865c2c3-d66b-407c-a9bc-8a25c9f2b20d", "openfda": {"unii": ["4BA73M5E37"], "rxcui": ["309309"], "spl_set_id": ["1057be77-00bb-4839-be3d-c8e11ae531a2"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE (50090-7848-1)", "package_ndc": "50090-7848-1", "marketing_start_date": "20260105"}], "brand_name": "Ciprofloxacin Hydrochloride", "product_id": "50090-7848_0865c2c3-d66b-407c-a9bc-8a25c9f2b20d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "50090-7848", "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"}