propafenone hydrochloride

Generic: propafenone hydrochloride

Labeler: upsher-smith laboratories, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name propafenone hydrochloride
Generic Name propafenone hydrochloride
Labeler upsher-smith laboratories, llc
Dosage Form CAPSULE, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

propafenone hydrochloride 225 mg/1

Manufacturer
Upsher-Smith Laboratories, LLC

Identifiers & Regulatory

Product NDC 0832-0740
Product ID 0832-0740_45afbac0-5c1a-ebc5-e063-6294a90a4d5e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA212744
Marketing Start 2020-06-25
Marketing End 2026-11-30

Pharmacologic Class

Classes
antiarrhythmic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 08320740
Hyphenated Format 0832-0740

Supplemental Identifiers

RxCUI
861156 861164 861171
UPC
0308320740607
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 ANDA212744 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 225 mg/1
source: ndc
Packaging
  • 60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0832-0740-60)
source: ndc

Packages (1)

0832-0740-60 60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0832-0740-60)

Ingredients (1)

propafenone hydrochloride (225 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": "45afbac0-5c1a-ebc5-e063-6294a90a4d5e", "openfda": {"upc": ["0308320740607"], "unii": ["33XCH0HOCD"], "rxcui": ["861156", "861164", "861171"], "spl_set_id": ["8aa6f58a-2980-4caa-9c54-d55d69d5d132"], "manufacturer_name": ["Upsher-Smith Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0832-0740-60)", "package_ndc": "0832-0740-60", "marketing_end_date": "20261031", "marketing_start_date": "20200625"}], "brand_name": "Propafenone Hydrochloride", "product_id": "0832-0740_45afbac0-5c1a-ebc5-e063-6294a90a4d5e", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Antiarrhythmic [EPC]"], "product_ndc": "0832-0740", "generic_name": "Propafenone Hydrochloride", "labeler_name": "Upsher-Smith Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Propafenone Hydrochloride", "active_ingredients": [{"name": "PROPAFENONE HYDROCHLORIDE", "strength": "225 mg/1"}], "application_number": "ANDA212744", "marketing_category": "ANDA", "marketing_end_date": "20261130", "marketing_start_date": "20200625"}