Package 68180-281-01

Brand: ethambutol hydrochloride

Generic: ethambutol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68180-281-01
Digits Only 6818028101
Product NDC 68180-281
Product ID 68180-281_b76b5b09-9d5d-4343-b128-0266024919b8
Description

100 TABLET in 1 BOTTLE (68180-281-01)

Marketing

Marketing Status
Marketed Since 2009-07-04
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": "b76b5b09-9d5d-4343-b128-0266024919b8", "openfda": {"upc": ["0368180281016", "0368180280019"], "unii": ["QE4VW5FO07"], "rxcui": ["995599", "995607"], "spl_set_id": ["c732b415-e1f9-478f-896d-1dc8b6362da4"], "manufacturer_name": ["Lupin Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68180-281-01)", "package_ndc": "68180-281-01", "marketing_start_date": "20090704"}], "brand_name": "Ethambutol Hydrochloride", "product_id": "68180-281_b76b5b09-9d5d-4343-b128-0266024919b8", "dosage_form": "TABLET", "pharm_class": ["Antimycobacterial [EPC]"], "product_ndc": "68180-281", "generic_name": "Ethambutol Hydrochloride", "labeler_name": "Lupin Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ethambutol Hydrochloride", "active_ingredients": [{"name": "ETHAMBUTOL HYDROCHLORIDE", "strength": "400 mg/1"}], "application_number": "ANDA078939", "marketing_category": "ANDA", "marketing_start_date": "20090704", "listing_expiration_date": "20261231"}