Package 51407-379-01

Brand: mexiletine hydrochloride

Generic: mexiletine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51407-379-01
Digits Only 5140737901
Product NDC 51407-379
Description

100 CAPSULE in 1 BOTTLE (51407-379-01)

Marketing

Marketing Status
Marketed Since 2020-12-18
Brand mexiletine hydrochloride
Generic mexiletine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "45b6d529-143e-2322-e063-6294a90a65a5", "openfda": {"unii": ["606D60IS38"], "rxcui": ["1362706", "1362712", "1362720"], "spl_set_id": ["bfe2b847-e18d-cef2-e053-2995a90a42af"], "manufacturer_name": ["Golden State Medical Supply, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (51407-379-01)", "package_ndc": "51407-379-01", "marketing_start_date": "20201218"}], "brand_name": "Mexiletine Hydrochloride", "product_id": "51407-379_45b6d529-143e-2322-e063-6294a90a65a5", "dosage_form": "CAPSULE", "pharm_class": ["Antiarrhythmic [EPC]"], "product_ndc": "51407-379", "generic_name": "Mexiletine Hydrochloride", "labeler_name": "Golden State Medical Supply, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mexiletine Hydrochloride", "active_ingredients": [{"name": "MEXILETINE HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA074450", "marketing_category": "ANDA", "marketing_start_date": "19960516", "listing_expiration_date": "20261231"}