NDC 0310-1830 – Fasenra

Benralizumab 30 mg/mL · Injection, Solution · Subcutaneous

Human Prescription Drug 1 recall

Product NDC0310-1830

Product details

Brand name
Fasenra
Generic name
Benralizumab
Labeler
AstraZeneca Pharmaceuticals LP
Dosage form
Injection, Solution
Route
Subcutaneous
Marketing category
BLA · BLA761070
Marketed since
October 4, 2019
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
0310-1830-301 CARTRIDGE in 1 CARTON (0310-1830-30) / 1 mL in 1 CARTRIDGEOct 4, 2019
0310-1830-85 sample1 CARTRIDGE in 1 CARTON (0310-1830-85) / 1 mL in 1 CARTRIDGEOct 4, 2019

Recalls mentioning this NDC

Other Fasenra products