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NDC 22840-5304, Xanthium strumarium, solution, from Greer Laboratories, Inc..

Product NDC
22840-5304
Status
Listed
Labeler
Greer Laboratories, Inc.
Dosage form
SOLUTION
Route
INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Product type
NON-STANDARDIZED ALLERGENIC
Marketing category
BLA
Application
BLA101833
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/22840-5304 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • XANTHIUM STRUMARIUM POLLEN.05 g/mL

Pharmacologic classes

Allergens [CS]; Cell-mediated Immunity [PE]; Increased Histamine Release [PE]; Increased IgG Production [PE]; Non-Standardized Pollen Allergenic Extract [EPC]; Pollen [CS]

Package NDCNDC-11Package
22840-5304-22284053040210 mL in 1 VIAL, MULTI-DOSE (22840-5304-2)
22840-5304-42284053040450 mL in 1 VIAL, MULTI-DOSE (22840-5304-4)
22840-5304-5228405304055 mL in 1 BOTTLE, DROPPER (22840-5304-5)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.

Use it

Look up 22840-5304 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/22840-5304 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 22840-5304. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.