NDC 0173-0892 – Nucala

Mepolizumab 100 mg/mL · Injection, Solution · Subcutaneous

Human Prescription Drug 1 recall

Product NDC0173-0892

Product details

Brand name
Nucala
Generic name
Mepolizumab
Labeler
GlaxoSmithKline LLC
Dosage form
Injection, Solution
Route
Subcutaneous
Marketing category
BLA · BLA761122
Marketed since
June 6, 2019
Listing expires
December 31, 2026
Pharmacologic class
Interleukin-5 Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Nucala →

Package NDC codes (4)

Package NDCDescriptionSince
0173-0892-011 SYRINGE in 1 CARTON (0173-0892-01) / 1 mL in 1 SYRINGEJun 6, 2019
0173-0892-421 SYRINGE in 1 CARTON (0173-0892-42) / 1 mL in 1 SYRINGEJun 6, 2019
0173-0892-611 SYRINGE in 1 CARTON (0173-0892-61) / 1 mL in 1 SYRINGEJun 6, 2019
0173-0892-631 SYRINGE in 1 CARTON (0173-0892-63) / 1 mL in 1 SYRINGEJun 6, 2019

Recalls mentioning this NDC

Other Nucala products