NDC 50474-970 – Briviact

Brivaracetam 50 mg/5mL · Injection, Suspension · Intravenous

Human Prescription Drug DEA schedule CV 1 recall

Product NDC50474-970

Product details

Brand name
Briviact
Generic name
Brivaracetam
Labeler
UCB, Inc.
Dosage form
Injection, Suspension
Route
Intravenous
Marketing category
NDA · NDA205837
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
50474-970-7510 VIAL, GLASS in 1 CARTON (50474-970-75) / 5 mL in 1 VIAL, GLASS (50474-970-63)May 12, 2016

Recalls mentioning this NDC

Other Briviact products