United States· US:49643-435_36ad1e17-751d-e226-e063-6394a90ab328

Red Alder Pollen

A medicinal product containing alnus rubra pollen, registered in United States by Allermed 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…normalisedRed Alder PollenATC—REGISTER NO.US:49643-435_36ad1e17…PACKS LISTED8CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
ALNUS RUBRA POLLEN
Manufacturer
Allermed 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
    49643-435-05
  • ndc11
    49643-435-10
  • ndc11
    49643-435-30
  • ndc11
    49643-435-50
  • ndc11
    4964343505
    5 mL in 1 VIAL, MULTI-DOSE (49643-435-05)
  • ndc11
    4964343510
    10 mL in 1 VIAL, MULTI-DOSE (49643-435-10)
  • ndc11
    4964343530
    30 mL in 1 VIAL, MULTI-DOSE (49643-435-30)
  • ndc11
    4964343550
    50 mL in 1 VIAL, MULTI-DOSE (49643-435-50)

Regulatory notes

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

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/ba3556a5-cdbc-4d8d-a0f7-4ed72febd045
GET /v1/drugs/ba3556a5-cdbc-4d8d-a0f7-4ed72febd045?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": "CUTANEOUS; INTRADERMAL; SUBCUTANEOUS",
  "source": "ndc",
  "strength": ".05",
  "substance": "ALNUS RUBRA POLLEN",
  "productndc": "49643-435",
  "dosage_form": "INJECTION",
  "dea_schedule": null,
  "strength_unit": "g/mL",
  "application_number": "BLA102211",
  "marketing_category": "BLA"
}

See everything about alnus rubra pollen.

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.