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Tuna

NDC 22840-5780 · Greer Laboratories, Inc.

Generic nameThunnus albacares
Dosage formSOLUTION
RouteINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active ingredient(s)YELLOWFIN TUNA
Strength.05 g/mL
Pharmacologic classAllergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Fish Proteins, Dietary [EXT], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC]
Marketing categoryBLA

Packages

22840-5780-2 — 10 mL in 1 VIAL, MULTI-DOSE (22840-5780-2)

22840-5780-5 — 5 mL in 1 BOTTLE, DROPPER (22840-5780-5)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

22840-9700 — Gadus morhua, Paralichthys lethostigma, Hippoglossus hippoglossus, Scomber scombrus and Thunnus albacares

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels