Package 10135-797-01

Brand: ethambutol hydrochloride

Generic: ethambutol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 10135-797-01
Digits Only 1013579701
Product NDC 10135-797
Product ID 10135-797_2dcb6b41-b9a8-4dde-8248-334d13f87a29
Description

100 TABLET, FILM COATED in 1 BOTTLE (10135-797-01)

Marketing

Marketing Status
Marketed Since 2025-08-26
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": "2dcb6b41-b9a8-4dde-8248-334d13f87a29", "openfda": {"unii": ["QE4VW5FO07"], "rxcui": ["995599", "995607"], "spl_set_id": ["1b9fbe16-edfc-44b6-b8d8-5c5a9d7558e1"], "manufacturer_name": ["Marlex Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (10135-797-01)", "package_ndc": "10135-797-01", "marketing_start_date": "20250826"}], "brand_name": "ETHAMBUTOL HYDROCHLORIDE", "product_id": "10135-797_2dcb6b41-b9a8-4dde-8248-334d13f87a29", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antimycobacterial [EPC]"], "product_ndc": "10135-797", "generic_name": "ETHAMBUTOL HYDROCHLORIDE", "labeler_name": "Marlex Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ETHAMBUTOL HYDROCHLORIDE", "active_ingredients": [{"name": "ETHAMBUTOL HYDROCHLORIDE", "strength": "400 mg/1"}], "application_number": "NDA016320", "marketing_category": "NDA", "marketing_start_date": "20061215", "listing_expiration_date": "20261231"}