Package 62559-820-01

Brand: mexiletine hydrochloride

Generic: mexiletine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 62559-820-01
Digits Only 6255982001
Product NDC 62559-820
Product ID 62559-820_2c6414d2-b1f3-4645-ae4f-5e5be0558e3f
Description

100 CAPSULE in 1 BOTTLE (62559-820-01)

Marketing

Marketing Status
Marketed Since 2020-06-22
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": "2c6414d2-b1f3-4645-ae4f-5e5be0558e3f", "openfda": {"upc": ["0362559820011", "0362559821018", "0362559822015"], "unii": ["606D60IS38"], "rxcui": ["1362706", "1362712", "1362720"], "spl_set_id": ["1b3a807f-368a-42dc-8266-ddf8347a8826"], "manufacturer_name": ["ANI Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (62559-820-01)", "package_ndc": "62559-820-01", "marketing_start_date": "20200622"}], "brand_name": "Mexiletine Hydrochloride", "product_id": "62559-820_2c6414d2-b1f3-4645-ae4f-5e5be0558e3f", "dosage_form": "CAPSULE", "pharm_class": ["Antiarrhythmic [EPC]"], "product_ndc": "62559-820", "generic_name": "Mexiletine Hydrochloride", "labeler_name": "ANI Pharmaceuticals, 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": "20200622", "listing_expiration_date": "20261231"}