propafenone hcl

Generic: propafenone hydrochloride

Labeler: actavis pharma, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name propafenone hcl
Generic Name propafenone hydrochloride
Labeler actavis pharma, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

propafenone hydrochloride 150 mg/1

Manufacturer
Actavis Pharma, Inc.

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
antiarrhythmic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 05910582
Hyphenated Format 0591-0582

Supplemental Identifiers

RxCUI
861424 861427
UNII
33XCH0HOCD

Packaging Origin

Original Packager
true

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
ORAL
source: ndc

Resolved Composition

Strengths
  • 150 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0591-0582-01)
source: ndc

Packages (1)

Ingredients (1)

propafenone hydrochloride (150 mg/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"}