Intravenous solutions with HEPARIN SODIUM IN SODIUM CHLORIDE INJECTION are supplied in single-dose flexible plastic containers in varied sizes and concentrations as shown in the accompanying Table.
Unit of Sale | Concentration |
NDC 0409-7650-62 Case of 24 Single-dose flexible plastic containers | 25,000 USP units/250 mL (100 USP units/mL) |
NDC 0409-7650-30 Case of 30 Single-dose flexible plastic containers | 25,000 USP units/250 mL (100 USP units/mL) |
NDC 0409-7651-62 Case of 24 Single-dose flexible plastic containers | 12,500 USP units/250 mL (50 USP units/mL) |
NDC 0409-0012-30 Case of 30 Single-dose flexible plastic containers | 12,500 USP units/250 mL (50 USP units/mL) |
NDC 0409-7651-03 Case of 24 Single-dose flexible plastic containers | 25,000 USP units/500 mL (50 USP units/mL) |
NDC 0409-3150-20 Case of 20 Single-dose flexible plastic containers | 25,000 USP units/500 mL (50 USP units/mL) |
Store at 20°C to 25°C (68°F to 77°F). [See USP Controlled Room Temperature.] Protect from freezing.
{{section_name_patient}}
{{section_body_html_patient}}
Additional Resources
Chat online with Pfizer Medical Information regarding your inquiry on a Pfizer medicine or vaccine.
Speak with a Pfizer Medical Information Professional regarding your Pfizer medicine or vaccine inquiry.
Available 9AM-5PM ET Monday to Friday; excluding holidays.
Submit a medical question for a Pfizer medicine or a vaccine.
The submission will be reviewed during our standard business hours.
To report an adverse event related to a Pfizer product and you are not part of a clinical trial* for this medication, click the link below to submit your information:
Pfizer Safety Reporting Site
*If you are involved in a clinical trial for either product, adverse events should be reported to your coordinating study site.
If you cannot use the above website to report an adverse event related to a Pfizer medication, please call (800) 438-1985.
You may also contact the U.S. Food and Drug Administration (FDA) directly to report adverse events or product quality concerns either online at www.fda.gov/medwatch or by calling (800) 332-1088.