50242-040 : Xolair 202.5 mg/1.4ml Subcutaneous Injection, Solution
NDC: | 50242-040 |
Labeler: | Genentech, Inc. |
Product Type: | Human Prescription Drug |
Drug Name: | Xolair |
Dosage Form: | Subcutaneous Injection, Solution |
Application #: | BLA103976 |
Rev. Date: |
NDC Package Codes:
- 50242-040-62: 1 VIAL, SINGLE‑USE IN 1 CARTON (50242‑040‑62) > 1.4 ML IN 1 VIAL, SINGLE‑USE
- 50242-040-86: 1 VIAL, SINGLE‑USE IN 1 CARTON (50242‑040‑86) > 1.4 ML IN 1 VIAL, SINGLE‑USE
Active Ingredients:
- Omalizumab
Dosage Strength:
- 202.5 mg/1.4mL
Pharmaceutical Classes:
- Anti-IgE [EPC]
- Decreased IgE Activity [PE]
- IgE-directed Antibody Interactions [MoA]
Related Products:
Based on records with the same trade name.- 50242-227 Xolair 300 mg/2ml Subcutaneous Injection, Solution by Genentech, Inc.
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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.