Package 63629-1963-1

Brand: mexiletine hydrochloride

Generic: mexiletine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63629-1963-1
Digits Only 6362919631
Product NDC 63629-1963
Product ID 63629-1963_03621bfd-3245-4fab-a7b5-0cc32f554485
Description

100 CAPSULE in 1 BOTTLE (63629-1963-1)

Marketing

Marketing Status
Marketed Since 2021-01-14
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": "03621bfd-3245-4fab-a7b5-0cc32f554485", "openfda": {"unii": ["606D60IS38"], "rxcui": ["1362712"], "spl_set_id": ["b1cb1e35-9586-41c4-b43f-c517f2d42f31"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (63629-1963-1)", "package_ndc": "63629-1963-1", "marketing_start_date": "20210114"}], "brand_name": "Mexiletine Hydrochloride", "product_id": "63629-1963_03621bfd-3245-4fab-a7b5-0cc32f554485", "dosage_form": "CAPSULE", "pharm_class": ["Antiarrhythmic [EPC]"], "product_ndc": "63629-1963", "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": "ANDA074450", "marketing_category": "ANDA", "marketing_start_date": "20200622", "listing_expiration_date": "20261231"}