Package 42291-624-01

Brand: mexiletine hydrochloride

Generic: mexiletine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 42291-624-01
Digits Only 4229162401
Product NDC 42291-624
Product ID 42291-624_4870f872-0804-7f08-e063-6394a90a19e9
Description

100 CAPSULE in 1 BOTTLE (42291-624-01)

Marketing

Marketing Status
Marketed Since 2013-07-09
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": "4870f872-0804-7f08-e063-6394a90a19e9", "openfda": {"upc": ["0342291625013"], "unii": ["606D60IS38"], "rxcui": ["1362706", "1362712", "1362720"], "spl_set_id": ["c528aae3-ff51-b9e4-a401-4ef5910e4b43"], "manufacturer_name": ["AvKARE"]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (42291-624-01)", "package_ndc": "42291-624-01", "marketing_start_date": "20130709"}], "brand_name": "Mexiletine Hydrochloride", "product_id": "42291-624_4870f872-0804-7f08-e063-6394a90a19e9", "dosage_form": "CAPSULE", "pharm_class": ["Antiarrhythmic [EPC]"], "product_ndc": "42291-624", "generic_name": "Mexiletine Hydrochloride", "labeler_name": "AvKARE", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mexiletine Hydrochloride", "active_ingredients": [{"name": "MEXILETINE HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA074377", "marketing_category": "ANDA", "marketing_start_date": "20130709", "listing_expiration_date": "20271231"}