Package 62135-785-90

Brand: mexiletine hydrochloride

Generic: mexiletine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 62135-785-90
Digits Only 6213578590
Product NDC 62135-785
Product ID 62135-785_462a5c01-c4ca-6bfa-e063-6294a90a4dd9
Description

90 CAPSULE in 1 BOTTLE (62135-785-90)

Marketing

Marketing Status
Marketed Since 2023-10-25
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": "462a5c01-c4ca-6bfa-e063-6294a90a4dd9", "openfda": {"upc": ["0362135785901"], "unii": ["606D60IS38"], "rxcui": ["1362720"], "spl_set_id": ["4e03e02f-c516-479e-9126-86b0df7f8b1c"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE in 1 BOTTLE (62135-785-90)", "package_ndc": "62135-785-90", "marketing_start_date": "20231025"}], "brand_name": "MEXILETINE HYDROCHLORIDE", "product_id": "62135-785_462a5c01-c4ca-6bfa-e063-6294a90a4dd9", "dosage_form": "CAPSULE", "pharm_class": ["Antiarrhythmic [EPC]"], "product_ndc": "62135-785", "generic_name": "mexiletine hydrochloride", "labeler_name": "Chartwell RX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "MEXILETINE HYDROCHLORIDE", "active_ingredients": [{"name": "MEXILETINE HYDROCHLORIDE", "strength": "250 mg/1"}], "application_number": "ANDA213500", "marketing_category": "ANDA", "marketing_start_date": "20200723", "listing_expiration_date": "20261231"}