Drug company (FDA labeler)
GVS TM Inc
Name in FDA records: GVS TM INC
NDC labeler code: 87069
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
- CP2D/AS-3 anticoagulant and additive systemLeukotrap Wb System - CP2D, Leukotrap Rc Pl System, Leukotrap Rc System · 12 products
- CPDA-1 blood bag collection systemLeukotrap Wb System · 3 products
- AS-32 products
FDA applications for these products
| Approved | Application | Medicine | Sponsor |
|---|---|---|---|
| — | BN800077 | CPDA-1 blood bag collection system | — |
| — | BN820915 | AS-3, CP2D/AS-3 anticoagulant and additive system | — |
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