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Rhizopus Mix

NDC 22840-9669, Rhizopus stolonifer and Rhizopus oryzae, solution, from Greer Laboratories, Inc..

Product NDC
22840-9669
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/22840-9669 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • RHIZOPUS STOLONIFER.0125 g/mL
  • RHIZOPUS ARRHIZUS.0125 g/mL

Pharmacologic classes

Allergens [CS]; Allergens [Chemical/Ingredient]; Cell-mediated Immunity [PE]; Cell-mediated Immunity [PE]; Fungal Proteins [CS]; Fungal Proteins [Chemical/Ingredient]; Increased Histamine Release [PE]; Increased Histamine Release [PE]; Increased IgG Production [PE]; Increased IgG Production [PE]; Non-Standardized Fungal Allergenic Extract [EPC]; Non-Standardized Fungal Allergenic Extract [EPC]

Package NDCNDC-11Package
22840-9669-22284096690210 mL in 1 VIAL, MULTI-DOSE (22840-9669-2)
22840-9669-42284096690450 mL in 1 VIAL, MULTI-DOSE (22840-9669-4)
22840-9669-5228409669055 mL in 1 BOTTLE, DROPPER (22840-9669-5)

Linked data

RxNorm, label and prices

RxNorm concepts

RxNorm links no concept to this product's packages.

Related lookups

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

Use it

Look up 22840-9669 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/22840-9669 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.