Package 82012-028-04

Brand: mexiletine hydrochloride

Generic: mexiletine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 82012-028-04
Digits Only 8201202804
Product NDC 82012-028
Product ID 82012-028_dd924d44-b14d-440c-9670-8faa42422ba1
Description

100 CAPSULE in 1 BOTTLE (82012-028-04)

Marketing

Marketing Status
Marketed Since 2021-11-29
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": "dd924d44-b14d-440c-9670-8faa42422ba1", "openfda": {"upc": ["0382012029041", "0382012027047", "0382012028044"], "unii": ["606D60IS38"], "rxcui": ["1362706", "1362712", "1362720"], "spl_set_id": ["c4a60f9e-fed1-4172-adc4-0be84ac65db9"], "manufacturer_name": ["Senores Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (82012-028-04)", "package_ndc": "82012-028-04", "marketing_start_date": "20211129"}], "brand_name": "MEXILETINE HYDROCHLORIDE", "product_id": "82012-028_dd924d44-b14d-440c-9670-8faa42422ba1", "dosage_form": "CAPSULE", "pharm_class": ["Antiarrhythmic [EPC]"], "product_ndc": "82012-028", "generic_name": "mexiletine hydrochloride", "labeler_name": "Senores Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "MEXILETINE HYDROCHLORIDE", "active_ingredients": [{"name": "MEXILETINE HYDROCHLORIDE", "strength": "200 mg/1"}], "application_number": "ANDA214089", "marketing_category": "ANDA", "marketing_start_date": "20211129", "listing_expiration_date": "20261231"}