NDC 0310-1745 – Fasenra

Benralizumab 10 mg/.5mL · Injection, Solution · Subcutaneous

Human Prescription Drug 1 recall

Product NDC0310-1745

Product details

Brand name
Fasenra
Generic name
Benralizumab
Labeler
AstraZeneca Pharmaceuticals LP
Dosage form
Injection, Solution
Route
Subcutaneous
Marketing category
BLA · BLA761070
Marketed since
April 5, 2024
Listing expires
December 31, 2027
Pharmacologic class
Interleukin-5 Receptor alpha-directed Cytolytic Antibody

Active ingredients

Uses, dosage, side effects and warnings for Fasenra →

Package NDC codes (2)

Package NDCDescriptionSince
0310-1745-011 CARTRIDGE in 1 CARTON (0310-1745-01) / .5 mL in 1 CARTRIDGEJun 3, 2024
0310-1745-95 sample1 CARTRIDGE in 1 CARTON (0310-1745-95) / .5 mL in 1 CARTRIDGEJun 3, 2024

Recalls mentioning this NDC

Other Fasenra products