Package 72162-1772-1

Brand: mexiletine hydrochloride

Generic: mexiletine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-1772-1
Digits Only 7216217721
Product NDC 72162-1772
Product ID 72162-1772_bc8628a2-a53e-48bf-9222-38693412e9ea
Description

100 CAPSULE in 1 BOTTLE (72162-1772-1)

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": "bc8628a2-a53e-48bf-9222-38693412e9ea", "openfda": {"unii": ["606D60IS38"], "rxcui": ["1362706"], "spl_set_id": ["9c2e1055-2fa1-462c-90f3-6d77e89ea38a"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (72162-1772-1)", "package_ndc": "72162-1772-1", "marketing_start_date": "20240207"}], "brand_name": "Mexiletine Hydrochloride", "product_id": "72162-1772_bc8628a2-a53e-48bf-9222-38693412e9ea", "dosage_form": "CAPSULE", "pharm_class": ["Antiarrhythmic [EPC]"], "product_ndc": "72162-1772", "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": "150 mg/1"}], "application_number": "ANDA074450", "marketing_category": "ANDA", "marketing_start_date": "20200622", "listing_expiration_date": "20261231"}