Package 54879-001-01

Brand: ethambutol hydrochloride

Generic: ethambutol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 54879-001-01
Digits Only 5487900101
Product NDC 54879-001
Product ID 54879-001_0ec564dd-5593-52ee-e063-6294a90a34de
Description

12 CARTON in 1 BOX (54879-001-01) / 12 BOTTLE in 1 CARTON / 100 TABLET, FILM COATED in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2006-12-15
Brand ethambutol hydrochloride
Generic ethambutol hydrochloride
Sample Package No

Linked Drug Pages (1)

Ethambutol Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0ec564dd-5593-52ee-e063-6294a90a34de", "openfda": {"unii": ["QE4VW5FO07"], "rxcui": ["995599", "995607"], "spl_set_id": ["3f6428d6-3745-4337-ad78-ebfff9f49135"], "manufacturer_name": ["STI Pharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "12 CARTON in 1 BOX (54879-001-01)  / 12 BOTTLE in 1 CARTON / 100 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "54879-001-01", "marketing_start_date": "20061215"}], "brand_name": "Ethambutol Hydrochloride", "product_id": "54879-001_0ec564dd-5593-52ee-e063-6294a90a34de", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antimycobacterial [EPC]"], "product_ndc": "54879-001", "generic_name": "Ethambutol Hydrochloride", "labeler_name": "STI Pharma LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ethambutol Hydrochloride", "active_ingredients": [{"name": "ETHAMBUTOL HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "NDA016320", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20061215", "listing_expiration_date": "20261231"}