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Neurospora intermedia

NDC 22840-1699 · Greer Laboratories, Inc.

Generic nameNeurospora intermedia
Dosage formSOLUTION
RouteINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active ingredient(s)NEUROSPORA INTERMEDIA
Strength.1 g/mL
Pharmacologic classAllergens [CS], Cell-mediated Immunity [PE], Fungal Proteins [CS], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Fungal Allergenic Extract [EPC]
Marketing categoryBLA

Packages

22840-1699-2 — 10 mL in 1 VIAL, MULTI-DOSE (22840-1699-2)

22840-1699-4 — 50 mL in 1 VIAL, MULTI-DOSE (22840-1699-4)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

22840-2600 — Neurospora intermedia, 22840-2601 — Neurospora intermedia, 22840-2602 — Neurospora intermedia, 22840-5627 — Neurospora intermedia, 22840-9642 — Candida albicans and Neurospora intermedia, 22840-9643 — Candida albicans and Neurospora intermedia, 22840-9644 — Candida albicans and Neurospora intermedia, 22840-9645 — Candida albicans and Neurospora intermedia, 22840-9677 — Candida albicans and Neurospora intermedia

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