Package 42806-101-01

Brand: ethambutol hydrochloride

Generic: ethambutol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 42806-101-01
Digits Only 4280610101
Product NDC 42806-101
Product ID 42806-101_a5247287-041a-4548-9a24-aadbfd233459
Description

100 TABLET, FILM COATED in 1 BOTTLE (42806-101-01)

Marketing

Marketing Status
Marketed Since 2020-07-30
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": "a5247287-041a-4548-9a24-aadbfd233459", "openfda": {"upc": ["0342806101018", "0342806102015"], "unii": ["QE4VW5FO07"], "rxcui": ["995599", "995607"], "spl_set_id": ["08decdf3-a397-42e7-8ac3-e489c0cc7085"], "manufacturer_name": ["Epic Pharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (42806-101-01)", "package_ndc": "42806-101-01", "marketing_start_date": "20200730"}], "brand_name": "ETHAMBUTOL HYDROCHLORIDE", "product_id": "42806-101_a5247287-041a-4548-9a24-aadbfd233459", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antimycobacterial [EPC]"], "product_ndc": "42806-101", "generic_name": "ETHAMBUTOL HYDROCHLORIDE", "labeler_name": "Epic Pharma, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ETHAMBUTOL HYDROCHLORIDE", "active_ingredients": [{"name": "ETHAMBUTOL HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA075095", "marketing_category": "ANDA", "marketing_start_date": "20150318", "listing_expiration_date": "20261231"}