Package 69238-2432-1

Brand: ciprofloxacin

Generic: ciprofloxacin
NDC Package

Package Facts

Identity

Package NDC 69238-2432-1
Digits Only 6923824321
Product NDC 69238-2432
Description

100 TABLET, FILM COATED in 1 BOTTLE (69238-2432-1)

Marketing

Marketing Status
Marketed Since 2024-02-29
Brand ciprofloxacin
Generic ciprofloxacin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "d44c6eb1-e419-4bee-977a-b1b46444595f", "openfda": {"unii": ["4BA73M5E37"], "rxcui": ["197511", "197512", "309309"], "spl_set_id": ["b996e81b-36ec-4ad7-a7c4-bc6700a06648"], "manufacturer_name": ["Amneal Pharmaceuticals NY LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (69238-2432-1)", "package_ndc": "69238-2432-1", "marketing_start_date": "20240229"}], "brand_name": "Ciprofloxacin", "product_id": "69238-2432_d44c6eb1-e419-4bee-977a-b1b46444595f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "69238-2432", "generic_name": "Ciprofloxacin", "labeler_name": "Amneal Pharmaceuticals NY LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ciprofloxacin", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "250 mg/1"}], "application_number": "ANDA075939", "marketing_category": "ANDA", "marketing_start_date": "20240229", "listing_expiration_date": "20261231"}