NDC 53746-735 – Felbamate

Felbamate 600 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC53746-735

Product details

Brand name
Felbamate
Generic name
Felbamate
Labeler
Amneal Pharmaceuticals of New York LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA201680
Marketed since
August 10, 2022
Listing expires
December 31, 2027
Pharmacologic class
Anti-epileptic Agent

Active ingredients

Uses, dosage, side effects and warnings for Felbamate →

Package NDC codes (3)

Package NDCDescriptionSince
53746-735-18180 TABLET in 1 BOTTLE (53746-735-18)Aug 10, 2022
53746-735-3030 TABLET in 1 BOTTLE (53746-735-30)Aug 10, 2022
53746-735-9090 TABLET in 1 BOTTLE (53746-735-90)Aug 10, 2022

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