Package 60687-709-01

Brand: propafenone hydrochloride

Generic: propafenone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60687-709-01
Digits Only 6068770901
Product NDC 60687-709
Product ID 60687-709_3f172eeb-8316-cdbc-e063-6394a90a1e86
Description

100 BLISTER PACK in 1 CARTON (60687-709-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-709-11)

Marketing

Marketing Status
Discontinued 2027-01-31
Brand propafenone hydrochloride
Generic propafenone hydrochloride
Sample Package No

Linked Drug Pages (1)

Propafenone Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3f172eeb-8316-cdbc-e063-6394a90a1e86", "openfda": {"unii": ["33XCH0HOCD"], "rxcui": ["861424"], "spl_set_id": ["343e4ad7-05e2-4e6c-8f8e-91c07739cae2"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (60687-709-01)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-709-11)", "package_ndc": "60687-709-01", "marketing_end_date": "20270131", "marketing_start_date": "20221013"}], "brand_name": "Propafenone Hydrochloride", "product_id": "60687-709_3f172eeb-8316-cdbc-e063-6394a90a1e86", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antiarrhythmic [EPC]"], "product_ndc": "60687-709", "generic_name": "Propafenone Hydrochloride", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Propafenone Hydrochloride", "active_ingredients": [{"name": "PROPAFENONE HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA075938", "marketing_category": "ANDA", "marketing_end_date": "20270131", "marketing_start_date": "20221013"}