Package 60687-778-21

Brand: mexiletine hydrochloride

Generic: mexiletine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60687-778-21
Digits Only 6068777821
Product NDC 60687-778
Product ID 60687-778_43551356-5d60-0b13-e063-6394a90a6cd7
Description

30 BLISTER PACK in 1 CARTON (60687-778-21) / 1 CAPSULE in 1 BLISTER PACK (60687-778-11)

Marketing

Marketing Status
Marketed Since 2024-02-23
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": "43551356-5d60-0b13-e063-6394a90a6cd7", "openfda": {"unii": ["606D60IS38"], "rxcui": ["1362706"], "spl_set_id": ["9d0b5d78-63dc-4208-b590-0789d3ed5785"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 CARTON (60687-778-21)  / 1 CAPSULE in 1 BLISTER PACK (60687-778-11)", "package_ndc": "60687-778-21", "marketing_start_date": "20240223"}], "brand_name": "Mexiletine hydrochloride", "product_id": "60687-778_43551356-5d60-0b13-e063-6394a90a6cd7", "dosage_form": "CAPSULE", "pharm_class": ["Antiarrhythmic [EPC]"], "product_ndc": "60687-778", "generic_name": "Mexiletine hydrochloride", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mexiletine hydrochloride", "active_ingredients": [{"name": "MEXILETINE HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA216463", "marketing_category": "ANDA", "marketing_start_date": "20240223", "listing_expiration_date": "20261231"}