NDC 72578-056 – Felbamate

Felbamate 400 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC72578-056

Product details

Brand name
Felbamate
Generic name
Felbamate
Labeler
Viona Pharmaceuticals Inc
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA208970
Marketed since
March 3, 2020
Listing expires
December 31, 2027
Pharmacologic class
Anti-epileptic Agent

Active ingredients

Uses, dosage, side effects and warnings for Felbamate →

Package NDC codes (5)

Package NDCDescriptionSince
72578-056-01100 TABLET in 1 BOTTLE (72578-056-01)Mar 3, 2020
72578-056-05500 TABLET in 1 BOTTLE (72578-056-05)Mar 3, 2020
72578-056-0630 TABLET in 1 BOTTLE (72578-056-06)Mar 3, 2020
72578-056-1690 TABLET in 1 BOTTLE (72578-056-16)Mar 3, 2020
72578-056-7710 BLISTER PACK in 1 CARTON (72578-056-77) / 10 TABLET in 1 BLISTER PACK (72578-056-30)Mar 3, 2020

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