propafenone hydrochloride
Generic: propafenone hydrochloride
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
propafenone hydrochloride
Generic Name
propafenone hydrochloride
Labeler
bryant ranch prepack
Dosage Form
TABLET, COATED
Routes
Active Ingredients
propafenone hydrochloride 225 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
63629-1988
Product ID
63629-1988_ff1cd958-1b7d-422c-bdfd-0fad7d98d6bc
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA076550
Listing Expiration
2026-12-31
Marketing Start
2015-03-31
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
636291988
Hyphenated Format
63629-1988
Supplemental Identifiers
RxCUI
UNII
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
source: ndc
Resolved Composition
Strengths
- 225 mg/1
Packaging
- 100 TABLET, COATED in 1 BOTTLE (63629-1988-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ff1cd958-1b7d-422c-bdfd-0fad7d98d6bc", "openfda": {"unii": ["33XCH0HOCD"], "rxcui": ["861427"], "spl_set_id": ["2492317c-8b04-477e-a5d2-53e791fface9"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, COATED in 1 BOTTLE (63629-1988-1)", "package_ndc": "63629-1988-1", "marketing_start_date": "20210202"}], "brand_name": "Propafenone Hydrochloride", "product_id": "63629-1988_ff1cd958-1b7d-422c-bdfd-0fad7d98d6bc", "dosage_form": "TABLET, COATED", "pharm_class": ["Antiarrhythmic [EPC]"], "product_ndc": "63629-1988", "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": "225 mg/1"}], "application_number": "ANDA076550", "marketing_category": "ANDA", "marketing_start_date": "20150331", "listing_expiration_date": "20261231"}