NDC 49401-102 – Benlysta

Belimumab 400 mg/5mL · Injection, Powder, Lyophilized, For Solution · Intravenous

Human Prescription Drug 1 recall

Product NDC49401-102

Product details

Brand name
Benlysta
Generic name
Belimumab
Labeler
GlaxoSmithKline LLC
Dosage form
Injection, Powder, Lyophilized, For Solution
Route
Intravenous
Marketing category
BLA · BLA125370
Marketed since
March 10, 2011
Listing expires
December 31, 2027
Pharmacologic class
B Lymphocyte Stimulator-specific Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Benlysta →

Package NDC codes (1)

Package NDCDescriptionSince
49401-102-011 VIAL in 1 CARTON (49401-102-01) / 5 mL in 1 VIALMar 10, 2011

Recalls mentioning this NDC

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