flecainide acetate

Generic: flecainide acetate

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name flecainide acetate
Generic Name flecainide acetate
Labeler a-s medication solutions
Dosage Form TABLET
Routes
ORAL
Active Ingredients

flecainide acetate 50 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-5306
Product ID 50090-5306_c97a62d4-b357-486d-a0be-6a87af13f749
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202821
Listing Expiration 2026-12-31
Marketing Start 2015-07-08

Pharmacologic Class

Classes
antiarrhythmic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500905306
Hyphenated Format 50090-5306

Supplemental Identifiers

RxCUI
886662
UNII
M8U465Q1WQ

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 flecainide acetate (source: ndc)
Generic Name flecainide acetate (source: ndc)
Application Number ANDA202821 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 60 TABLET in 1 BOTTLE (50090-5306-0)
source: ndc

Packages (1)

Ingredients (1)

flecainide acetate (50 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "c97a62d4-b357-486d-a0be-6a87af13f749", "openfda": {"unii": ["M8U465Q1WQ"], "rxcui": ["886662"], "spl_set_id": ["475a52a9-f18c-4a69-91f0-8f5e601f4336"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (50090-5306-0)", "package_ndc": "50090-5306-0", "marketing_start_date": "20201028"}], "brand_name": "Flecainide Acetate", "product_id": "50090-5306_c97a62d4-b357-486d-a0be-6a87af13f749", "dosage_form": "TABLET", "pharm_class": ["Antiarrhythmic [EPC]"], "product_ndc": "50090-5306", "generic_name": "Flecainide Acetate", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Flecainide Acetate", "active_ingredients": [{"name": "FLECAINIDE ACETATE", "strength": "50 mg/1"}], "application_number": "ANDA202821", "marketing_category": "ANDA", "marketing_start_date": "20150708", "listing_expiration_date": "20261231"}