Drugplain

NDC 53746-735-18

Felbamate 600 mg/1

Felbamate · TABLET

No Recall History

Felbamate is a tablet containing felbamate at a strength of 600 mg/1. Manufactured by Amneal Pharmaceuticals of New York LLC.

Key Facts

Brand Name
Felbamate
Generic Name
Felbamate
NDC Code (Package)
53746-735-18
NDC Code (Product)
53746-735
Manufacturer
Amneal Pharmaceuticals of New York LLC
Strength
600 mg/1
Dosage Form
TABLET
Route
ORAL
Marketing Status
Application #
ANDA201680
Drug Class
Anti-epileptic Agent [EPC]
Marketing Start
08/10/2022

Recall History

No Recall History

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Felbamate — All Packages

Not medical advice. This information is for reference only. Always consult your doctor or pharmacist.