Package 61442-223-05

Brand: ciprofloxacin

Generic: ciprofloxacin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 61442-223-05
Digits Only 6144222305
Product NDC 61442-223
Product ID 61442-223_2d6a2060-1f59-696d-e063-6394a90a2796
Description

500 TABLET, FILM COATED in 1 BOTTLE (61442-223-05)

Marketing

Marketing Status
Marketed Since 2009-10-10
Brand ciprofloxacin
Generic ciprofloxacin hydrochloride
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": "2d6a2060-1f59-696d-e063-6394a90a2796", "openfda": {"upc": ["0361442222017", "0361442223014", "0361442224509"], "unii": ["4BA73M5E37"], "rxcui": ["197511", "197512", "309309"], "spl_set_id": ["37527eca-115e-4582-88cd-bba851ac6069"], "manufacturer_name": ["Carlsbad Technology, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (61442-223-01)", "package_ndc": "61442-223-01", "marketing_start_date": "20091010"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (61442-223-05)", "package_ndc": "61442-223-05", "marketing_start_date": "20091010"}], "brand_name": "Ciprofloxacin", "product_id": "61442-223_2d6a2060-1f59-696d-e063-6394a90a2796", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "61442-223", "generic_name": "Ciprofloxacin Hydrochloride", "labeler_name": "Carlsbad Technology, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ciprofloxacin", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA076126", "marketing_category": "ANDA", "marketing_start_date": "20091010", "listing_expiration_date": "20261231"}