United States · FDA National Drug Code directory

Flecainide Acetate

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
63629-1945_53e01a4a-d6ee-4f76-94ce-40fbede5eeae
Product NDC
63629-1945
Form
TABLET
Composition / generic term
Flecainide Acetate Tablet
Labeler
Bryant Ranch Prepack
Marketing category
ANDA
Marketing start / end (source format)
20151228
Source listing expiry
20261231

Source-listed ingredients

  • FLECAINIDE ACETATE — 100 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 TABLET in 1 BOTTLE (63629-1945-1) · 63629-1945-1

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

Browse United States records →