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Drug Information for ENBREL (etanercept) For Subcutaneous Injection (Immunex Corp): PACKAGE LABEL - PRINCIPAL DISPLAY PANEL - PREFILLED SYRINGE, 50 MG
- DESCRIPTION
- INDICATIONS AND USAGE
- CONTRAINDICATIONS
- WARNINGS
- OVERDOSAGE
- HOW SUPPLIED
- REFERENCES
- Medication GuideENBREL® (en-brel)(etanercept)
- Patient Instructions for UseENBREL® (en-brel)(etanercept)Single-use Prefilled Syringe
- Patient Instructions for UseENBREL® (en-brel)(etanercept)Multiple-use Vial
- Patient Instructions for UseENBREL® (en-brel)(etanercept)Single-use Prefilled SureClick™ Autoinjector
- PACKAGE LABEL - PRINCIPAL DISPLAY PANEL - PREFILLED SYRINGE, 25 MG
- PACKAGE LABEL - PRINCIPAL DISPLAY PANEL - PREFILLED SYRINGE, 50 MG
- PACKAGE LABEL - PRINCIPAL DISPLAY PANEL - PREFILLED AUTOINJECTOR, 50 MG
- PACKAGE LABEL - PRINCIPAL DISPLAY PANEL - VIAL, 25 MG
- External Links Related to ENBREL (etanercept) For Subcutaneous Injection (Immunex Corp)
Contains 4 Single-use Prefilled Syringes
NDC 58406-435-04
Enbrel®
etanercept
50 mg/mL
Single-use Prefilled Syringe
50 mg
Attention: Not for use in pediatric patients under 138 lbs.
For Subcutaneous Use Only
Refrigerate at 2° to 8°C (36° to 46°F). DO NOT FREEZE.
Each single-use prefilled syringe contains 0.98 mL of a clear and colorless solution containing 50 mg/mL etanercept and is formulated at pH 6.3 ± 0.2, with 1% sucrose, 100 mM sodium chloride, 25 mM L-arginine hydrochloride, and 25 mM sodium phosphate.
Specific activity: approximately 1.7 x 106 U/mg.
Manufactured by Immunex Corporation, Thousand Oaks, CA 91320
U.S. License No. 1132
Marketed by Amgen and Wyeth Pharmaceuticals
©2004 Immunex Corporation
Immunex U.S. Patent Numbers: 5,695,760; 5,605,690; 5,945,397; 6,201,105; Re. 36,755

- Drug Information Provided by National Library of Medicine (NLM).