Package 0832-0740-60

Brand: propafenone hydrochloride

Generic: propafenone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0832-0740-60
Digits Only 0832074060
Product NDC 0832-0740
Description

60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0832-0740-60)

Marketing

Marketing Status
Discontinued 2026-10-31
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": "45afbac0-5c1a-ebc5-e063-6294a90a4d5e", "openfda": {"upc": ["0308320740607"], "unii": ["33XCH0HOCD"], "rxcui": ["861156", "861164", "861171"], "spl_set_id": ["8aa6f58a-2980-4caa-9c54-d55d69d5d132"], "manufacturer_name": ["Upsher-Smith Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0832-0740-60)", "package_ndc": "0832-0740-60", "marketing_end_date": "20261031", "marketing_start_date": "20200625"}], "brand_name": "Propafenone Hydrochloride", "product_id": "0832-0740_45afbac0-5c1a-ebc5-e063-6294a90a4d5e", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Antiarrhythmic [EPC]"], "product_ndc": "0832-0740", "generic_name": "Propafenone Hydrochloride", "labeler_name": "Upsher-Smith Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Propafenone Hydrochloride", "active_ingredients": [{"name": "PROPAFENONE HYDROCHLORIDE", "strength": "225 mg/1"}], "application_number": "ANDA212744", "marketing_category": "ANDA", "marketing_end_date": "20261130", "marketing_start_date": "20200625"}