NDC 72789-385 – Flecainide Acetate

Flecainide Acetate 50 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC72789-385

Product details

Brand name
Flecainide Acetate
Generic name
Flecainide acetate
Labeler
PD-Rx Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA210683
Marketed since
January 11, 2024
Listing expires
December 31, 2027
Pharmacologic class
Antiarrhythmic

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
72789-385-01100 TABLET in 1 BOTTLE, PLASTIC (72789-385-01)Feb 27, 2024
72789-385-6060 TABLET in 1 BOTTLE, PLASTIC (72789-385-60)Feb 27, 2024
72789-385-93180 TABLET in 1 BOTTLE, PLASTIC (72789-385-93)Feb 27, 2024

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