Skip to main content

Xanthoxylum Fraxineum

NDC 37662-2410 · Hahnemann Laboratories, INC.

Generic nameXanthoxylum Fraxineum
Dosage formPELLET
RouteORAL
Active ingredient(s)ZANTHOXYLUM AMERICANUM BARK
Strength1 [hp_M]/1
Marketing categoryUNAPPROVED HOMEOPATHIC

Packages

37662-2410-1 — 200 PELLET in 1 VIAL, GLASS (37662-2410-1)

37662-2410-2 — 500 PELLET in 1 VIAL, GLASS (37662-2410-2)

37662-2410-3 — 3000 PELLET in 1 BOTTLE, GLASS (37662-2410-3)

37662-2410-4 — 10000 PELLET in 1 BOTTLE, GLASS (37662-2410-4)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0220-5335 — ZANTHOXYLUM AMERICANUM BARK, 0220-5336 — ZANTHOXYLUM AMERICANUM BARK, 37662-2404 — Xanthoxylum Fraxineum, 37662-2405 — Xanthoxylum Fraxineum, 37662-2406 — Xanthoxylum Fraxineum, 37662-2407 — Xanthoxylum Fraxineum, 37662-2408 — Xanthoxylum Fraxineum, 37662-2409 — Xanthoxylum Fraxineum, 37662-2411 — Xanthoxylum Fraxineum, 37662-2412 — Xanthoxylum Fraxineum, 58264-0217 — Formica rufa, POTASSIUM CARBONATE, KALMIA LATIFOLIA WHOLE, ZANTHOXYLUM AMERICANUM BARK, and BOS TAURUS PARATHYROID GLAND

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