Package 71335-2780-2

Brand: propafenone hydrochloride

Generic: propafenone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-2780-2
Digits Only 7133527802
Product NDC 71335-2780
Description

90 TABLET, COATED in 1 BOTTLE (71335-2780-2)

Marketing

Marketing Status
Marketed Since 2025-10-13
Brand propafenone hydrochloride
Generic propafenone hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "8091654a-d552-41b3-b090-2ae99ef6dee3", "openfda": {"unii": ["33XCH0HOCD"], "rxcui": ["861424"], "spl_set_id": ["617faff7-d9e4-477d-ab2c-aded5c129a86"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE (71335-2780-1)", "package_ndc": "71335-2780-1", "marketing_start_date": "20251013"}, {"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE (71335-2780-2)", "package_ndc": "71335-2780-2", "marketing_start_date": "20251013"}], "brand_name": "Propafenone Hydrochloride", "product_id": "71335-2780_8091654a-d552-41b3-b090-2ae99ef6dee3", "dosage_form": "TABLET, COATED", "pharm_class": ["Antiarrhythmic [EPC]"], "product_ndc": "71335-2780", "generic_name": "Propafenone Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Propafenone Hydrochloride", "active_ingredients": [{"name": "PROPAFENONE HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA076550", "marketing_category": "ANDA", "marketing_start_date": "20150331", "listing_expiration_date": "20261231"}