Package 63629-9181-1

Brand: mexiletine hydrochloride

Generic: mexiletine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63629-9181-1
Digits Only 6362991811
Product NDC 63629-9181
Product ID 63629-9181_e4e4a99f-c012-4701-9df1-dbf824017a41
Description

100 CAPSULE in 1 BOTTLE (63629-9181-1)

Marketing

Marketing Status
Marketed Since 2022-02-22
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": "e4e4a99f-c012-4701-9df1-dbf824017a41", "openfda": {"unii": ["606D60IS38"], "rxcui": ["1362720"], "spl_set_id": ["217fbd7a-1052-42e4-9e84-70519b7b0b7a"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (63629-9181-1)", "package_ndc": "63629-9181-1", "marketing_start_date": "20220222"}], "brand_name": "MEXILETINE HYDROCHLORIDE", "product_id": "63629-9181_e4e4a99f-c012-4701-9df1-dbf824017a41", "dosage_form": "CAPSULE", "pharm_class": ["Antiarrhythmic [EPC]"], "product_ndc": "63629-9181", "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"}