Kali Telluricosum

NDC 37662-3338 · Hahnemann Laboratories, INC.

Generic nameKali Telluricosum

Dosage formPELLET

RouteORAL

Active ingredient(s)POTASSIUM TELLURITE

Strength100 [hp_C]/1

Pharmacologic classIncreased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC]

Marketing categoryUNAPPROVED HOMEOPATHIC

Packages

37662-3338-1 — 200 PELLET in 1 VIAL, GLASS (37662-3338-1)

37662-3338-2 — 500 PELLET in 1 VIAL, GLASS (37662-3338-2)

37662-3338-3 — 3000 PELLET in 1 BOTTLE, GLASS (37662-3338-3)

37662-3338-4 — 10000 PELLET in 1 BOTTLE, GLASS (37662-3338-4)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

37662-3335 — Kali Telluricosum, 37662-3336 — Kali Telluricosum, 37662-3337 — Kali Telluricosum, 37662-3339 — Kali Telluricosum, 37662-3340 — Kali Telluricosum, 37662-3341 — Kali Telluricosum, 37662-3342 — Kali Telluricosum

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