Package 16729-491-12

Brand: dofetilide

Generic: dofetilide
NDC Package

Package Facts

Identity

Package NDC 16729-491-12
Digits Only 1672949112
Product NDC 16729-491
Description

60 CAPSULE in 1 BOTTLE (16729-491-12)

Marketing

Marketing Status
Marketed Since 2020-08-20
Brand dofetilide
Generic dofetilide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "40bca241-47f2-b7f0-e063-6294a90a1680", "openfda": {"nui": ["N0000175426"], "unii": ["R4Z9X1N2ND"], "rxcui": ["310003", "310004", "310005"], "spl_set_id": ["4c1a5a6d-bd69-473c-8caa-d0d242b7708d"], "pharm_class_epc": ["Antiarrhythmic [EPC]"], "manufacturer_name": ["Accord Healthcare, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 CAPSULE in 1 BOTTLE (16729-491-12)", "package_ndc": "16729-491-12", "marketing_start_date": "20200820"}], "brand_name": "Dofetilide", "product_id": "16729-491_40bca241-47f2-b7f0-e063-6294a90a1680", "dosage_form": "CAPSULE", "pharm_class": ["Antiarrhythmic [EPC]"], "product_ndc": "16729-491", "generic_name": "Dofetilide", "labeler_name": "Accord Healthcare, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dofetilide", "active_ingredients": [{"name": "DOFETILIDE", "strength": ".25 mg/1"}], "application_number": "ANDA213338", "marketing_category": "ANDA", "marketing_start_date": "20200820", "listing_expiration_date": "20261231"}