United States · FDA National Drug Code directory
Tuna
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 22840-5780_36abfd47-fc5e-43c4-e063-6394a90a8731
- Product NDC
- 22840-5780
- Form
- SOLUTION
- Composition / generic term
- Thunnus albacares
- Labeler
- Greer Laboratories, Inc.
- Marketing category
- BLA
- Marketing start / end (source format)
- 19810915
- Source listing expiry
- 20261231
Source-listed ingredients
- YELLOWFIN TUNA — .05 g/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 10 mL in 1 VIAL, MULTI-DOSE (22840-5780-2) · 22840-5780-2
- 5 mL in 1 BOTTLE, DROPPER (22840-5780-5) · 22840-5780-5
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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