propafenone hydrochloride
Generic: propafenone hydrochloride
Labeler: strides pharma science limitedDrug Facts
Product Profile
Brand Name
propafenone hydrochloride
Generic Name
propafenone hydrochloride
Labeler
strides pharma science limited
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
propafenone hydrochloride 300 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
64380-246
Product ID
64380-246_e3779c96-a513-4375-857e-bbe3b2532d64
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA075938
Listing Expiration
2026-12-31
Marketing Start
2025-05-05
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
64380246
Hyphenated Format
64380-246
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 300 mg/1
Packaging
- 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (64380-246-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "e3779c96-a513-4375-857e-bbe3b2532d64", "openfda": {"upc": ["0364380246015", "0364380268024", "0364380269021"], "unii": ["33XCH0HOCD"], "rxcui": ["861424", "861427", "861430"], "spl_set_id": ["c65253ab-937f-4982-b841-69c2b9f9ccdb"], "manufacturer_name": ["Strides Pharma Science Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (64380-246-01)", "package_ndc": "64380-246-01", "marketing_start_date": "20250505"}], "brand_name": "PROPAFENONE HYDROCHLORIDE", "product_id": "64380-246_e3779c96-a513-4375-857e-bbe3b2532d64", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antiarrhythmic [EPC]"], "product_ndc": "64380-246", "generic_name": "PROPAFENONE HYDROCHLORIDE", "labeler_name": "Strides Pharma Science Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PROPAFENONE HYDROCHLORIDE", "active_ingredients": [{"name": "PROPAFENONE HYDROCHLORIDE", "strength": "300 mg/1"}], "application_number": "ANDA075938", "marketing_category": "ANDA", "marketing_start_date": "20250505", "listing_expiration_date": "20261231"}