Package 62756-956-01

Brand: mexiletine hydrochloride

Generic: mexiletine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 62756-956-01
Digits Only 6275695601
Product NDC 62756-956
Product ID 62756-956_7bb96934-8c07-463e-b96e-cafaafb8d2dc
Description

100 CAPSULE in 1 BOTTLE (62756-956-01)

Marketing

Marketing Status
Marketed Since 2021-11-29
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": "7bb96934-8c07-463e-b96e-cafaafb8d2dc", "openfda": {"unii": ["606D60IS38"], "rxcui": ["1362706", "1362712", "1362720"], "spl_set_id": ["2d0c61ca-4c99-42f9-8f00-e0e9d2672a39"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (62756-956-01)", "package_ndc": "62756-956-01", "marketing_start_date": "20211129"}], "brand_name": "MEXILETINE HYDROCHLORIDE", "product_id": "62756-956_7bb96934-8c07-463e-b96e-cafaafb8d2dc", "dosage_form": "CAPSULE", "pharm_class": ["Antiarrhythmic [EPC]"], "product_ndc": "62756-956", "generic_name": "mexiletine hydrochloride", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "MEXILETINE HYDROCHLORIDE", "active_ingredients": [{"name": "MEXILETINE HYDROCHLORIDE", "strength": "200 mg/1"}], "application_number": "ANDA214089", "marketing_category": "ANDA", "marketing_start_date": "20211129", "listing_expiration_date": "20261231"}