Package 72162-1773-1

Brand: mexiletine hydrochloride

Generic: mexiletine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-1773-1
Digits Only 7216217731
Product NDC 72162-1773
Product ID 72162-1773_b32e1416-4347-47ea-a4ed-69983070e7ef
Description

100 CAPSULE in 1 BOTTLE (72162-1773-1)

Marketing

Marketing Status
Marketed Since 2024-02-07
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": "b32e1416-4347-47ea-a4ed-69983070e7ef", "openfda": {"unii": ["606D60IS38"], "rxcui": ["1362712"], "spl_set_id": ["a0bd3f2c-44e5-4ad0-9b76-c2028f0cae11"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (72162-1773-1)", "package_ndc": "72162-1773-1", "marketing_start_date": "20240207"}], "brand_name": "Mexiletine Hydrochloride", "product_id": "72162-1773_b32e1416-4347-47ea-a4ed-69983070e7ef", "dosage_form": "CAPSULE", "pharm_class": ["Antiarrhythmic [EPC]"], "product_ndc": "72162-1773", "generic_name": "Mexiletine Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mexiletine Hydrochloride", "active_ingredients": [{"name": "MEXILETINE HYDROCHLORIDE", "strength": "200 mg/1"}], "application_number": "ANDA074450", "marketing_category": "ANDA", "marketing_start_date": "20200622", "listing_expiration_date": "20261231"}