Package 0527-4109-37

Brand: mexiletine hydrochloride

Generic: mexiletine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0527-4109-37
Digits Only 0527410937
Product NDC 0527-4109
Product ID 0527-4109_8da7d3ff-0e0c-4401-8ced-81bbc16c230b
Description

100 CAPSULE in 1 BOTTLE (0527-4109-37)

Marketing

Marketing Status
Marketed Since 2020-07-23
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": "8da7d3ff-0e0c-4401-8ced-81bbc16c230b", "openfda": {"upc": ["0305274107371", "0305274109375", "0305274108378"], "unii": ["606D60IS38"], "rxcui": ["1362706", "1362712", "1362720"], "spl_set_id": ["4cf19b14-050e-4083-8f1e-6618310e02f1"], "manufacturer_name": ["Lannett Company, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (0527-4109-37)", "package_ndc": "0527-4109-37", "marketing_start_date": "20200723"}], "brand_name": "Mexiletine Hydrochloride", "product_id": "0527-4109_8da7d3ff-0e0c-4401-8ced-81bbc16c230b", "dosage_form": "CAPSULE", "pharm_class": ["Antiarrhythmic [EPC]"], "product_ndc": "0527-4109", "generic_name": "Mexiletine Hydrochloride", "labeler_name": "Lannett Company, Inc.", "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"}