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
- 63629-7982_1a02594a-dc61-44e8-939f-41786366f079
- Product NDC
- 63629-7982
- Form
- TABLET
- Composition / generic term
- Flecainide Acetate
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20150708
- Source listing expiry
- 20261231
Source-listed ingredients
- FLECAINIDE ACETATE — 100 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET in 1 BOTTLE (63629-7982-1) · 63629-7982-1
- 60 TABLET in 1 BOTTLE (63629-7982-2) · 63629-7982-2
- 90 TABLET in 1 BOTTLE (63629-7982-3) · 63629-7982-3
- 180 TABLET in 1 BOTTLE (63629-7982-4) · 63629-7982-4
Source and coverage
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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.
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