propafenone hydrochloride

Generic: propafenone hydrochloride

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name propafenone hydrochloride
Generic Name propafenone hydrochloride
Labeler bryant ranch prepack
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

propafenone hydrochloride 150 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-2780
Product ID 71335-2780_8091654a-d552-41b3-b090-2ae99ef6dee3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076550
Listing Expiration 2026-12-31
Marketing Start 2015-03-31

Pharmacologic Class

Classes
antiarrhythmic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713352780
Hyphenated Format 71335-2780

Supplemental Identifiers

RxCUI
861424
UNII
33XCH0HOCD

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 ANDA076550 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 150 mg/1
source: ndc
Packaging
  • 30 TABLET, COATED in 1 BOTTLE (71335-2780-1)
  • 90 TABLET, COATED in 1 BOTTLE (71335-2780-2)
source: ndc

Packages (2)

71335-2780-1 30 TABLET, COATED in 1 BOTTLE (71335-2780-1) 71335-2780-2 90 TABLET, COATED in 1 BOTTLE (71335-2780-2)

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": "8091654a-d552-41b3-b090-2ae99ef6dee3", "openfda": {"unii": ["33XCH0HOCD"], "rxcui": ["861424"], "spl_set_id": ["617faff7-d9e4-477d-ab2c-aded5c129a86"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE (71335-2780-1)", "package_ndc": "71335-2780-1", "marketing_start_date": "20251013"}, {"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE (71335-2780-2)", "package_ndc": "71335-2780-2", "marketing_start_date": "20251013"}], "brand_name": "Propafenone Hydrochloride", "product_id": "71335-2780_8091654a-d552-41b3-b090-2ae99ef6dee3", "dosage_form": "TABLET, COATED", "pharm_class": ["Antiarrhythmic [EPC]"], "product_ndc": "71335-2780", "generic_name": "Propafenone Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Propafenone Hydrochloride", "active_ingredients": [{"name": "PROPAFENONE HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA076550", "marketing_category": "ANDA", "marketing_start_date": "20150331", "listing_expiration_date": "20261231"}