Package 72162-1784-1

Brand: mexiletine hydrochloride

Generic: mexiletine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-1784-1
Digits Only 7216217841
Product NDC 72162-1784
Product ID 72162-1784_19b815db-4a55-462d-a7c1-5fa18ab97789
Description

100 CAPSULE in 1 BOTTLE (72162-1784-1)

Marketing

Marketing Status
Marketed Since 2024-04-04
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": "19b815db-4a55-462d-a7c1-5fa18ab97789", "openfda": {"unii": ["606D60IS38"], "rxcui": ["1362720"], "spl_set_id": ["0ff45dbf-b555-4f55-a286-98bfaea9ea29"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (72162-1784-1)", "package_ndc": "72162-1784-1", "marketing_start_date": "20240404"}], "brand_name": "MEXILETINE HYDROCHLORIDE", "product_id": "72162-1784_19b815db-4a55-462d-a7c1-5fa18ab97789", "dosage_form": "CAPSULE", "pharm_class": ["Antiarrhythmic [EPC]"], "product_ndc": "72162-1784", "generic_name": "mexiletine hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "MEXILETINE HYDROCHLORIDE", "active_ingredients": [{"name": "MEXILETINE HYDROCHLORIDE", "strength": "250 mg/1"}], "application_number": "ANDA214089", "marketing_category": "ANDA", "marketing_start_date": "20211129", "listing_expiration_date": "20261231"}