Package 72162-1783-1

Brand: mexiletine hydrochloride

Generic: mexiletine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-1783-1
Digits Only 7216217831
Product NDC 72162-1783
Product ID 72162-1783_59f978d8-bfa3-4f24-8d3f-7e3ff0741954
Description

100 CAPSULE in 1 BOTTLE (72162-1783-1)

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": "59f978d8-bfa3-4f24-8d3f-7e3ff0741954", "openfda": {"unii": ["606D60IS38"], "rxcui": ["1362712"], "spl_set_id": ["2f4239ef-a28a-40d3-9617-2029d492829d"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (72162-1783-1)", "package_ndc": "72162-1783-1", "marketing_start_date": "20240404"}], "brand_name": "MEXILETINE HYDROCHLORIDE", "product_id": "72162-1783_59f978d8-bfa3-4f24-8d3f-7e3ff0741954", "dosage_form": "CAPSULE", "pharm_class": ["Antiarrhythmic [EPC]"], "product_ndc": "72162-1783", "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": "200 mg/1"}], "application_number": "ANDA214089", "marketing_category": "ANDA", "marketing_start_date": "20211129", "listing_expiration_date": "20261231"}