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Ambrosia artemisiaefolia

NDC 0220-0218 · Boiron

Generic nameAMBROSIA ARTEMISIIFOLIA

Dosage formPELLET

RouteORAL

Active ingredient(s)AMBROSIA ARTEMISIIFOLIA

Strength6 [hp_C]/6[hp_C]

Marketing categoryUNAPPROVED HOMEOPATHIC

Packages

0220-0218-41 — 6 [hp_C] in 1 TUBE (0220-0218-41)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0220-0219 — AMBROSIA ARTEMISIIFOLIA, 0220-0230 — AMBROSIA ARTEMISIIFOLIA, 0268-1483 — AMBROSIA ARTEMISIIFOLIA AND AMBROSIA TRIFIDA POLLEN, 0268-8056 — AMBROSIA ARTEMISIIFOLIA and AMBROSIA TRIFIDA POLLEN, 0268-8059 — AMBROSIA ARTEMISIIFOLIA, AMBROSIA TRIFIDA POLLEN, 0268-8060 — AMBROSIA ARTEMISIIFOLIA, AMBROSIA TRIFIDA POLLEN

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