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United States· US:49643-343_36ad5f03-e686-f1d0-e063-6394a90adfe8

Standardized Orchard Grass

A medicinal product containing dactylis glomerata 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…normalisedStandardized Orchard GrassATC—REGISTER NO.US:49643-343_36ad5f03…PACKS LISTED8CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
DACTYLIS GLOMERATA 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
    4964334305
    5 mL in 1 VIAL, MULTI-DOSE (49643-343-05)
  • ndc11
    4964334310
    10 mL in 1 VIAL, MULTI-DOSE (49643-343-10)
  • ndc11
    4964334330
    30 mL in 1 VIAL, MULTI-DOSE (49643-343-30)
  • ndc11
    4964334350
    50 mL in 1 VIAL, MULTI-DOSE (49643-343-50)
  • ndc11
    49643-343-05
  • ndc11
    49643-343-10
  • ndc11
    49643-343-30
  • ndc11
    49643-343-50

Regulatory notes

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

Same medicine, other countries

Dactylis glomerata pollen in 1 other country

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

All dactylis glomerata pollen products

Authorised across Europe · EMA

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

  • Netherlands · Pollen Bencard, Prick Test Pollen Hal Allergy

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/63516a1f-5681-438b-a08d-3be3f7a916ce
GET /v1/drugs/63516a1f-5681-438b-a08d-3be3f7a916ce?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": "100000",
  "substance": "DACTYLIS GLOMERATA POLLEN",
  "productndc": "49643-343",
  "dosage_form": "INJECTION",
  "dea_schedule": null,
  "strength_unit": "[BAU]/mL",
  "application_number": "BLA102217",
  "marketing_category": "BLA"
}

See everything about dactylis glomerata 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.