propafenone hydrochloride

Generic: propafenone hydrochloride

Labeler: aurobindo pharma limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name propafenone hydrochloride
Generic Name propafenone hydrochloride
Labeler aurobindo pharma limited
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

propafenone hydrochloride 150 mg/1

Manufacturer
Aurobindo Pharma Limited

Identifiers & Regulatory

Product NDC 59651-256
Product ID 59651-256_b59b252f-8b73-4f72-8d01-4d2076c18fa6
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202445
Listing Expiration 2026-12-31
Marketing Start 2019-10-25

Pharmacologic Class

Classes
antiarrhythmic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 59651256
Hyphenated Format 59651-256

Supplemental Identifiers

RxCUI
861424 861427 861430
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 hydrochloride (source: ndc)
Generic Name propafenone hydrochloride (source: ndc)
Application Number ANDA202445 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 150 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (59651-256-01)
  • 300 TABLET, FILM COATED in 1 BOTTLE (59651-256-33)
source: ndc

Packages (2)

59651-256-01 100 TABLET, FILM COATED in 1 BOTTLE (59651-256-01) 59651-256-33 300 TABLET, FILM COATED in 1 BOTTLE (59651-256-33)

Ingredients (1)

propafenone hydrochloride (150 mg/1)

Linked Drug Pages (1)

PROPAFENONE HYDROCHLORIDE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "b59b252f-8b73-4f72-8d01-4d2076c18fa6", "openfda": {"unii": ["33XCH0HOCD"], "rxcui": ["861424", "861427", "861430"], "spl_set_id": ["0c887381-42fe-4f37-858a-d9ffb218dd1c"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (59651-256-01)", "package_ndc": "59651-256-01", "marketing_start_date": "20191025"}, {"sample": false, "description": "300 TABLET, FILM COATED in 1 BOTTLE (59651-256-33)", "package_ndc": "59651-256-33", "marketing_start_date": "20191025"}], "brand_name": "PROPAFENONE HYDROCHLORIDE", "product_id": "59651-256_b59b252f-8b73-4f72-8d01-4d2076c18fa6", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antiarrhythmic [EPC]"], "product_ndc": "59651-256", "generic_name": "PROPAFENONE HYDROCHLORIDE", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PROPAFENONE HYDROCHLORIDE", "active_ingredients": [{"name": "PROPAFENONE HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA202445", "marketing_category": "ANDA", "marketing_start_date": "20191025", "listing_expiration_date": "20261231"}