Package 69367-385-01

Brand: ciprofloxacin hydrochloride

Generic: ciprofloxacin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 69367-385-01
Digits Only 6936738501
Product NDC 69367-385
Product ID 69367-385_e679760f-b4d3-4a21-9d47-40c2355bc2c0
Description

100 TABLET, FILM COATED in 1 BOTTLE (69367-385-01)

Marketing

Marketing Status
Marketed Since 2024-05-23
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": "e679760f-b4d3-4a21-9d47-40c2355bc2c0", "openfda": {"upc": ["0369367386012"], "unii": ["4BA73M5E37"], "rxcui": ["197511", "197512", "309309"], "spl_set_id": ["c47250c2-bece-46b5-8b3b-b7c97d9005d8"], "manufacturer_name": ["Westminster Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (69367-385-01)", "package_ndc": "69367-385-01", "marketing_start_date": "20240523"}], "brand_name": "Ciprofloxacin Hydrochloride", "product_id": "69367-385_e679760f-b4d3-4a21-9d47-40c2355bc2c0", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "69367-385", "generic_name": "Ciprofloxacin Hydrochloride", "labeler_name": "Westminster Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ciprofloxacin Hydrochloride", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "250 mg/1"}], "application_number": "ANDA076593", "marketing_category": "ANDA", "marketing_start_date": "20240523", "listing_expiration_date": "20261231"}