Package 62559-231-01
Brand: propafenone hydrochloride
Generic: propafenone hydrochloridePackage Facts
Identity
Package NDC
62559-231-01
Digits Only
6255923101
Product NDC
62559-231
Description
100 TABLET, COATED in 1 BOTTLE (62559-231-01)
Marketing
Marketing Status
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": "f3d9c704-c65d-43cd-aafd-2aebe4abfee3", "openfda": {"upc": ["0362559231015", "0362559230018", "0362559232012"], "unii": ["33XCH0HOCD"], "rxcui": ["861424", "861427", "861430"], "spl_set_id": ["8d1be333-be2b-4064-86a4-c2ad9ad07b83"], "manufacturer_name": ["ANI Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, COATED in 1 BOTTLE (62559-231-01)", "package_ndc": "62559-231-01", "marketing_start_date": "20150331"}], "brand_name": "Propafenone Hydrochloride", "product_id": "62559-231_f3d9c704-c65d-43cd-aafd-2aebe4abfee3", "dosage_form": "TABLET, COATED", "pharm_class": ["Antiarrhythmic [EPC]"], "product_ndc": "62559-231", "generic_name": "Propafenone Hydrochloride", "labeler_name": "ANI Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Propafenone Hydrochloride", "active_ingredients": [{"name": "PROPAFENONE HYDROCHLORIDE", "strength": "225 mg/1"}], "application_number": "ANDA076550", "marketing_category": "ANDA", "marketing_start_date": "20150331", "listing_expiration_date": "20261231"}