NDC 50242-040 – Xolair
Omalizumab 150 mg/1.2mL · Injection, Solution · Subcutaneous
Product NDC50242-040
Product details
- Brand name
- Xolair
- Generic name
- Omalizumab
- Labeler
- Genentech, Inc.
- Dosage form
- Injection, Solution
- Route
- Subcutaneous
- Marketing category
- BLA · BLA103976
- Marketed since
- June 20, 2003
- Listing expires
- December 31, 2027
- Pharmacologic class
- Anti-IgE
Active ingredients
- Omalizumab 150 mg/1.2mL
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 50242-040-62 | 1 VIAL, SINGLE-USE in 1 CARTON (50242-040-62) / 1.2 mL in 1 VIAL, SINGLE-USE | Jun 20, 2003 |
| 50242-040-86 sample | 1 VIAL, SINGLE-USE in 1 CARTON (50242-040-86) / 1.2 mL in 1 VIAL, SINGLE-USE | Dec 20, 2013 |
Recalls mentioning this NDC
- D-0571-2025 Aug 13, 2025 · Class II
CGMP Deviations - Product was exposed to temperatures outside the product's labeled storage requirements. - D-0572-2025 Aug 13, 2025 · Class II
CGMP Deviations - Product was exposed to temperatures outside the product's labeled storage requirements. - D-0650-2021 Jul 14, 2021 · Class II
Failed Stability Specifications: Out of Specification results of Polysorbate 20 (PS20) content were detected at the 12 month testing time point.
Other Xolair products
- 50242-227 Omalizumab 300 mg/2mL · Injection, Solution · Genentech, Inc.