Package 64980-667-01

Brand: mexiletine hydrochloride

Generic: mexiletine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 64980-667-01
Digits Only 6498066701
Product NDC 64980-667
Product ID 64980-667_17c65cba-f56f-4cad-a9e2-d31f62e95849
Description

100 CAPSULE in 1 BOTTLE (64980-667-01)

Marketing

Marketing Status
Marketed Since 2025-02-05
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": "17c65cba-f56f-4cad-a9e2-d31f62e95849", "openfda": {"unii": ["606D60IS38"], "rxcui": ["1362706", "1362712", "1362720"], "spl_set_id": ["17c65cba-f56f-4cad-a9e2-d31f62e95849"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (64980-667-01)", "package_ndc": "64980-667-01", "marketing_start_date": "20250205"}], "brand_name": "Mexiletine Hydrochloride", "product_id": "64980-667_17c65cba-f56f-4cad-a9e2-d31f62e95849", "dosage_form": "CAPSULE", "pharm_class": ["Antiarrhythmic [EPC]"], "product_ndc": "64980-667", "generic_name": "Mexiletine Hydrochloride", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mexiletine Hydrochloride", "active_ingredients": [{"name": "MEXILETINE HYDROCHLORIDE", "strength": "200 mg/1"}], "application_number": "ANDA215315", "marketing_category": "ANDA", "marketing_start_date": "20250205", "listing_expiration_date": "20261231"}