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Laurocerasus

NDC 37662-1750 · Hahnemann Laboratories, INC.

Generic nameLaurocerasus
Dosage formPELLET
RouteORAL
Active ingredient(s)PRUNUS LAUROCERASUS LEAF
Strength6 [hp_C]/1
Marketing categoryUNAPPROVED HOMEOPATHIC

Packages

37662-1750-1 — 200 PELLET in 1 VIAL, GLASS (37662-1750-1)

37662-1750-2 — 1200 PELLET in 1 BOTTLE, GLASS (37662-1750-2)

37662-1750-3 — 4000 PELLET in 1 BOTTLE, GLASS (37662-1750-3)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0220-2994 — PRUNUS LAUROCERASUS LEAF, 0220-3069 — PRUNUS LAUROCERASUS LEAF, 37662-1751 — Laurocerasus, 37662-1752 — Laurocerasus, 37662-1753 — Laurocerasus, 37662-1754 — Laurocerasus, 37662-1755 — Laurocerasus, 37662-1756 — Laurocerasus, 37662-1757 — Laurocerasus, 37662-1758 — Laurocerasus, 58264-0044 — CRATAEGUS LAEVIGATA FRUIT, PRUNUS LAUROCERASUS LEAF, NERIUM OLEANDER LEAF, and CYTISUS SCOPARIUS WHOLE, 82969-2239 — China off, Crataegus, Laurocerasus, Oleander, Scoparium

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