propafenone hydrochloride

Generic: propafenone hydrochloride

Labeler: american health packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name propafenone hydrochloride
Generic Name propafenone hydrochloride
Labeler american health packaging
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

propafenone hydrochloride 150 mg/1

Manufacturer
American Health Packaging

Identifiers & Regulatory

Product NDC 60687-930
Product ID 60687-930_41b16e34-8b2c-19d5-e063-6394a90a8d7e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075938
Listing Expiration 2026-12-31
Marketing Start 2025-10-21

Pharmacologic Class

Classes
antiarrhythmic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 60687930
Hyphenated Format 60687-930

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 ANDA075938 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 150 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 CARTON (60687-930-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-930-11)
source: ndc

Packages (1)

60687-930-01 100 BLISTER PACK in 1 CARTON (60687-930-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-930-11)

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": "41b16e34-8b2c-19d5-e063-6394a90a8d7e", "openfda": {"unii": ["33XCH0HOCD"], "rxcui": ["861424"], "spl_set_id": ["da08c286-b930-463a-858a-efc54f12019f"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (60687-930-01)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-930-11)", "package_ndc": "60687-930-01", "marketing_start_date": "20251021"}], "brand_name": "PROPAFENONE HYDROCHLORIDE", "product_id": "60687-930_41b16e34-8b2c-19d5-e063-6394a90a8d7e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antiarrhythmic [EPC]"], "product_ndc": "60687-930", "generic_name": "PROPAFENONE HYDROCHLORIDE", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PROPAFENONE HYDROCHLORIDE", "active_ingredients": [{"name": "PROPAFENONE HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA075938", "marketing_category": "ANDA", "marketing_start_date": "20251021", "listing_expiration_date": "20261231"}