Generic drug makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of ViatrisLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record. See the Viatris group view.
As of Nov 14, 2026, FDA's public records list Dey Laboratories, Inc. with 6 510(k) clearances. The most recent is a 510(k) clearance dated Oct 8, 1997: DEY VIAL SODIUM CHLORIDE 3%.
| Oct 8, 1997 | DEY VIAL SODIUM CHLORIDE 3%K972778 · CAF | 510(k) clearances |
| May 22, 1991 | NEBU-SOL METERED DOSE DISPENSER (TM)K910239 · BSY | 510(k) clearances |
| Feb 29, 1988 | DEY-VIAL SODIUM CHLORIDE SOLUTION, USP, STERILEK880411 · CAF | 510(k) clearances |
| Jan 22, 1988 | DEY-PAK AND DEY-VIAL SODIUM CHLORIDE SOLUTION, USPK875024 · CCQ | 510(k) clearances |
| Jan 22, 1988 | DEY-PAK PURIFIED WATER, USP, STERILEK875011 · CCQ | 510(k) clearances |
| Jul 12, 1983 | OCULAR IRRIGATING CANNULAK831532 · HMX | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
