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United States· US:37662-1141_e537e1fc-3b8a-8ce1-e053-2a95a90a8005

Melilotus Officinalis

A medicinal product containing melilotus officinalis top, registered in United States by Hahnemann Laboratories, INC..

US label

Checked against FDA National Drug Code directory (United States) on

Informational only — not a medical device.

SOURCE REGISTER · USFDA National Drug Code directory (Unite…normalisedMelilotus OfficinalisATC—REGISTER NO.US:37662-1141_e537e1f…PACKS LISTED8CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
MELILOTUS OFFICINALIS TOP
Manufacturer
Hahnemann Laboratories, INC.
Country
United States (US)
ATC code
—
Reimbursed
Not published by this register
Source register
FDA National Drug Code directory (United States)
Last checked
September 27, 2026

Packs & prices · 8

  • ndc11
    37662-1141-1
  • ndc11
    37662-1141-2
  • ndc11
    37662-1141-3
  • ndc11
    37662-1141-4
  • ndc11
    3766211411
    80 PELLET in 1 VIAL, GLASS (37662-1141-1)
  • ndc11
    3766211412
    200 PELLET in 1 VIAL, GLASS (37662-1141-2)
  • ndc11
    3766211413
    1200 PELLET in 1 BOTTLE, GLASS (37662-1141-3)
  • ndc11
    3766211414
    4000 PELLET in 1 BOTTLE, GLASS (37662-1141-4)

Regulatory notes

No shortage, Orange Book or US label notes for this record.

Same medicine, other countries

Melilotus officinalis top in 1 other country

What each register calls a product with the same active substance — salts and hydrates count as the same.

All melilotus officinalis top products

Authorised across Europe · EMA

The same active substance is authorised in 1 EEA country. Names it is sold under:

  • Poland · Plaster Nostrzykowy

Source: European Medicines Agency, Article 57 product data.

Sourced from a public register and reproduced with attribution. Drug Database is not affiliated with, endorsed by, or a partner of FDA National Drug Code directory (United States). This is an informational data service and not a medical device — verify against the official source of record before any clinical decision.

For developers

The same record over the API, and the raw payload
GET /v1/drugs/dc914923-7c61-4c77-a099-3e8330337cb9
GET /v1/drugs/dc914923-7c61-4c77-a099-3e8330337cb9?format=fhir

Every response carries last_synced_at, so freshness is a field rather than a promise. Below is exactly what the ingestion wrote, before any presentation — the same JSON the API returns under payload.

{
  "route": "ORAL",
  "source": "ndc",
  "strength": "30",
  "substance": "MELILOTUS OFFICINALIS TOP",
  "productndc": "37662-1141",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "strength_unit": "[hp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC"
}

See everything about melilotus officinalis top.

This page is the registration. A free account adds the label text as the regulator wrote it, what it costs per daily dose across the markets that publish a price, a feed of what changes in the registers, and an assistant that answers with its sources. Interaction severity is free; mechanism and management are on the Growth plan. No card, nothing to install.