IMOVAX RABIES
RABIES VIRUS STRAIN PM-1503-3M ANTIGEN (PROPIOLACTONE INACTIVATED) and WATER · KIT · Sanofi Vaccines US Inc.
IMOVAX RABIES is a kit containing rabies virus strain pm-1503-3m antigen (propiolactone inactivated) and water. Manufactured by Sanofi Vaccines US Inc..
Key Facts
- Brand Name
- IMOVAX RABIES
- Generic Name
- RABIES VIRUS STRAIN PM-1503-3M ANTIGEN (PROPIOLACTONE INACTIVATED) and WATER
- NDC Code (Product)
49281-252- Manufacturer
- Sanofi Vaccines US Inc.
- Dosage Form
- KIT
- Marketing Status
- Application #
- BLA103931
- Marketing Start
- 10/25/2019
Recall History
No Recall HistoryFrequently Asked Questions
What is IMOVAX RABIES used for?
IMOVAX RABIES contains RABIES VIRUS STRAIN PM-1503-3M ANTIGEN (PROPIOLACTONE INACTIVATED) and WATER. It is a kit taken as directed. Consult your doctor for specific uses.
Is IMOVAX RABIES a controlled substance?
IMOVAX RABIES is not classified as a controlled substance by the DEA.
What is the generic name for IMOVAX RABIES?
The generic name for IMOVAX RABIES is RABIES VIRUS STRAIN PM-1503-3M ANTIGEN (PROPIOLACTONE INACTIVATED) and WATER. There are no other listed brand versions of RABIES VIRUS STRAIN PM-1503-3M ANTIGEN (PROPIOLACTONE INACTIVATED) and WATER.
What is the NDC code for IMOVAX RABIES ?
The NDC (National Drug Code) for IMOVAX RABIES is 49281-252, listed by Sanofi Vaccines US Inc..
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)