NDC 50474-870 – Briviact

Brivaracetam 10 mg/mL · Solution · Oral

Human Prescription Drug DEA schedule CV 1 recall

Product NDC50474-870

Product details

Brand name
Briviact
Generic name
Brivaracetam
Labeler
UCB, Inc.
Dosage form
Solution
Route
Oral
Marketing category
NDA · NDA205838
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
50474-870-151 BOTTLE in 1 CARTON (50474-870-15) / 300 mL in 1 BOTTLEMay 12, 2016

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