Package 50742-240-01

Brand: mexiletine hydrochloride

Generic: mexiletine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50742-240-01
Digits Only 5074224001
Product NDC 50742-240
Product ID 50742-240_64851116-6653-4b86-9bc0-24f93b4ece10
Description

100 CAPSULE in 1 BOTTLE (50742-240-01)

Marketing

Marketing Status
Marketed Since 2021-01-26
Brand mexiletine hydrochloride
Generic mexiletine hydrochloride
Sample Package No

Linked Drug Pages (1)

MEXILETINE HYDROCHLORIDE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "64851116-6653-4b86-9bc0-24f93b4ece10", "openfda": {"upc": ["0350742239016", "0350742240012", "0350742241019"], "unii": ["606D60IS38"], "rxcui": ["1362706", "1362712", "1362720"], "spl_set_id": ["6dbf86f7-2b2d-40fb-868b-ee7d7a95556e"], "manufacturer_name": ["Ingenus Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (50742-240-01)", "package_ndc": "50742-240-01", "marketing_start_date": "20210126"}], "brand_name": "MEXILETINE HYDROCHLORIDE", "product_id": "50742-240_64851116-6653-4b86-9bc0-24f93b4ece10", "dosage_form": "CAPSULE", "pharm_class": ["Antiarrhythmic [EPC]"], "product_ndc": "50742-240", "generic_name": "Mexiletine hydrochloride", "labeler_name": "Ingenus Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "MEXILETINE HYDROCHLORIDE", "active_ingredients": [{"name": "MEXILETINE HYDROCHLORIDE", "strength": "200 mg/1"}], "application_number": "ANDA214352", "marketing_category": "ANDA", "marketing_start_date": "20210126", "listing_expiration_date": "20261231"}