Package 63629-2145-1

Brand: mexiletine hydrochloride

Generic: mexiletine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63629-2145-1
Digits Only 6362921451
Product NDC 63629-2145
Product ID 63629-2145_3410eae8-3459-4a3d-a0c5-04f159c6d140
Description

100 CAPSULE in 1 BOTTLE (63629-2145-1)

Marketing

Marketing Status
Marketed Since 2021-02-08
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": "3410eae8-3459-4a3d-a0c5-04f159c6d140", "openfda": {"unii": ["606D60IS38"], "rxcui": ["1362706"], "spl_set_id": ["c09f68fa-759e-4772-9f6b-11005d8f83d5"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (63629-2145-1)", "package_ndc": "63629-2145-1", "marketing_start_date": "20210208"}], "brand_name": "Mexiletine Hydrochloride", "product_id": "63629-2145_3410eae8-3459-4a3d-a0c5-04f159c6d140", "dosage_form": "CAPSULE", "pharm_class": ["Antiarrhythmic [EPC]"], "product_ndc": "63629-2145", "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"}