NDC 71335-3063 – Flecainide Acetate

Flecainide Acetate 100 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-3063

Product details

Brand name
Flecainide Acetate
Generic name
Flecainide acetate
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA215599
Marketed since
September 15, 2022
Listing expires
December 31, 2027
Pharmacologic class
Antiarrhythmic

Active ingredients

Uses, dosage, side effects and warnings for Flecainide Acetate →

Package NDC codes (5)

Package NDCDescriptionSince
71335-3063-130 TABLET in 1 BOTTLE (71335-3063-1)Feb 6, 2026
71335-3063-260 TABLET in 1 BOTTLE (71335-3063-2)Feb 6, 2026
71335-3063-390 TABLET in 1 BOTTLE (71335-3063-3)Feb 6, 2026
71335-3063-4180 TABLET in 1 BOTTLE (71335-3063-4)Feb 6, 2026
71335-3063-5100 TABLET in 1 BOTTLE (71335-3063-5)Feb 6, 2026

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