Drug company (FDA labeler)
Sintetica US LLC
NDC labeler code: 83090
What is a labeler?
The company whose name is on the package and in the FDA’s National Drug Code (NDC) Directory. It may make the medicine itself or sell medicine made by another company. The first part of every NDC code identifies the labeler.
Official FDA data only
Products, approvals and recalls come from the FDA (NDC Directory, Drugs@FDA, enforcement reports). Recalls are linked to this company by the NDC labeler code on the recalled product.
Questions about your medicine: ask your doctor or pharmacist. In an emergency, call 911.
Prescription medicines
- Arsenic trioxideTrisenox · 2 products
- DaptomycinDapzura Rt · 1 product
- LacosamideVimpat, Motpoly XR · 1 product
- BortezomibBoruzu, Velcade · 1 product
FDA applications for these products
- ANDA: Abbreviated New Drug Application: how a generic version is approved.
| Approved | Application | Medicine | Sponsor |
|---|---|---|---|
| February 13, 2024 | ANDA217311 | Lacosamide LACOSAMIDE | Hainan Poly |
| April 20, 2023 | ANDA217413 | Arsenic trioxide ARSENIC TRIOXIDE | Msn |
| August 18, 2022 | ANDA215890 | Daptomycin DAPTOMYCIN | Hainan Poly Pharm |
| July 26, 2022 | ANDA209622 | Bortezomib BORTEZOMIB | Msn |
The sponsor is the company that holds the FDA application; it can differ from the labeler.
Recall timeline
No recall of these products (by NDC code) appears in the FDA enforcement reports.
Next steps
- Find a pharmacy near youAsk which company made your medicine and whether it is recalled
- Latest FDA drug recallsAll companies, newest first
- All drug companiesA to Z
- All prescription drugs A to ZSearch by generic, brand or Spanish name
Sources
- NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026