NDC 50474-670 – Briviact

Brivaracetam 75 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug DEA schedule CV 1 recall

Product NDC50474-670

Product details

Brand name
Briviact
Generic name
Brivaracetam
Labeler
UCB, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
NDA · NDA205836
Marketed since
May 12, 2016
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Briviact →

Package NDC codes (1)

Package NDCDescriptionSince
50474-670-661 BOTTLE in 1 CARTON (50474-670-66) / 60 TABLET, FILM COATED in 1 BOTTLEMay 12, 2016

Recalls mentioning this NDC

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