NDC 50090-1079
CLOSTRIDIUM TETANI TOXOID ANTIGEN (FORMALDEHYDE INACTIVATED), CORYNEBACTERIUM DIPHTHERIAE TOXOID ANTIGEN (FORMALDEHYDE INACTIVATED), BORDETELLA PERTUSSIS TOXOID ANTIGEN (GLUTARALDEHYDE INACTIVATED), BORDETELLA PERTUSSIS FILAMENTOUS HEMAGGLUTININ ANTIGEN (FORMALDEHYDE INACTIVATED), BORDETELLA PERTUSSIS PERTACTIN ANTIGEN, and BORDETELLA PERTUSSIS FIMBRIAE 2/3 ANTIGEN 6 ingredients injection, suspension
On the label: A-S Medication Solutions. It's repackaged: A-S Medication Solutions rebottles it from Sanofi Vaccines US Inc.'s NDC 49281-400.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Sanofi Vaccines Canada Ltd. | North York, Canada | Makes it | Not inspected on record |
Repackaging site
- A-S Medication Solutions LLC, Libertyville, IL, United States · relabels it
Product details
- Generic drug
- Clostridium Tetani Toxoid Antigen (formaldehyde Inactivated), Corynebacterium Di: every company that makes it
- Form
- injection, suspension, intramuscular
- Strength
- 6 ingredients
- Approval
- BLA BLA125111
- On the market since
- Jun 10, 2005
- Package NDCs
50090-1079-050090-1079-1- Official label
- DailyMed (National Library of Medicine), updated Oct 22, 2023
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