propafenone hcl
Generic: propafenone hydrochloride
Labeler: actavis pharma, inc.Drug Facts
Product Profile
Brand Name
propafenone hcl
Generic Name
propafenone hydrochloride
Labeler
actavis pharma, inc.
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
propafenone hydrochloride 150 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0591-0582
Product ID
0591-0582_2e5ad1da-4d1b-4ebc-a9af-6d4d7d1cc97d
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA075203
Marketing Start
2000-10-24
Marketing End
2026-06-30
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
05910582
Hyphenated Format
0591-0582
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
propafenone hcl (source: ndc)
Generic Name
propafenone hydrochloride (source: ndc)
Application Number
ANDA075203 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 150 mg/1
Packaging
- 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0591-0582-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2e5ad1da-4d1b-4ebc-a9af-6d4d7d1cc97d", "openfda": {"unii": ["33XCH0HOCD"], "rxcui": ["861424", "861427"], "spl_set_id": ["a313c111-e539-47bc-9d57-c3767f74bcca"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0591-0582-01)", "package_ndc": "0591-0582-01", "marketing_end_date": "20260630", "marketing_start_date": "20001024"}], "brand_name": "Propafenone HCl", "product_id": "0591-0582_2e5ad1da-4d1b-4ebc-a9af-6d4d7d1cc97d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antiarrhythmic [EPC]"], "product_ndc": "0591-0582", "generic_name": "Propafenone hydrochloride", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Propafenone HCl", "active_ingredients": [{"name": "PROPAFENONE HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA075203", "marketing_category": "ANDA", "marketing_end_date": "20260630", "marketing_start_date": "20001024"}