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Aconitum napellus

NDC 63545-735 · Hahnemann Laboratories, Inc.

FDA carries 4 listing records for this NDC; the most recent is shown.

Generic nameAconitum napellus
Dosage formPELLET
RouteORAL
Active ingredient(s)ACONITUM NAPELLUS
Strength200 [hp_C]/1
Marketing categoryUNAPPROVED HOMEOPATHIC

Packages

63545-735-02 — 500 PELLET in 1 VIAL, GLASS (63545-735-02)

63545-735-04 — 10000 PELLET in 1 BOTTLE, GLASS (63545-735-04)

63545-735-03 — 3000 PELLET in 1 BOTTLE, GLASS (63545-735-03)

63545-735-01 — 200 PELLET in 1 VIAL, GLASS (63545-735-01)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

58264-0070 — ACONITUM NAPELLUS, SIMABA CEDRON SEED, CITRULLUS COLOCYNTHIS FRUIT PULP, KALMIA LATIFOLIA LEAF, and VERBASCUM THAPSUS, 58264-0071 — Aconitum napellus, Arsenic Trioxide, Citrullus Colocynthis Fruit Pulp, Pseudognaphalium Obtusifolium, and Magnesium Phosphate, Dibasic…, 60986-2035 — ACONITUM NAPELLUS, BELLADONNA, CHAMOMILLA, 60986-2040 — ACONITUM NAPELLUS, BRYONIA CRETICA, 62106-1141 — Arnica montana, Aconitum napellus, Gelsemium sempervirens, Aurum metallicum, Cuprum metallicum, 62795-1015 — ATROPINE SULFATE, ACONITUM NAPELLUS, BRYONIA ALBA ROOT, CITRULLUS COLOCYNTHIS FRUIT PULP, and CUPRIC SULFATE, 63545-144 — Aconitum napellus, 63545-732 — Aconitum napellus, 63545-733 — Aconitum napellus, 63545-734 — Aconitum napellus, 63545-736 — Aconitum napellus, 63545-737 — Aconitum napellus, 63545-738 — Aconitum napellus, 63545-739 — Aconitum napellus, 64578-0083 — Aconitum Napellus, Belladonna, Bryonia (Alba), Chamomilla, 66096-777 — ACONITUM NAPELLUS, 66343-082 — Aconitum napellus, Anacardium orientale, Cerebrum, Hypericum perforatum, 68466-1008 — ACONITUM NAPELLUS, BRYONIA ALBA ROOT, CALCIUM CATION, SPONGIA OFFICINALIS SKELETON, ROASTED, TIN, 68466-4098 — ACONITUM NAPELLUS, CALCIUM SULFIDE, SPONGIA OFFICINALIS SKELETON, ROASTED, TIN, 68703-315 — Aconitum nap, Lycopodium, Nat mur, Nux vom, Pulsatilla, +34 more

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