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United States· US:49643-048_36ad1e17-751d-e226-e063-6394a90ab328

Cockroach, German

A medicinal product containing blattella germanica, registered in United States by Allermed Laboratories, Inc..

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

Informational only — not a medical device.

SOURCE REGISTER · USFDA National Drug Code directory (Unite…normalisedCockroach, GermanATC—REGISTER NO.US:49643-048_36ad1e17…PACKS LISTED8CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
BLATTELLA GERMANICA
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
    49643-048-05
  • ndc11
    49643-048-10
  • ndc11
    49643-048-30
  • ndc11
    49643-048-50
  • ndc11
    4964304805
    5 mL in 1 VIAL, MULTI-DOSE (49643-048-05)
  • ndc11
    4964304810
    10 mL in 1 VIAL, MULTI-DOSE (49643-048-10)
  • ndc11
    4964304830
    30 mL in 1 VIAL, MULTI-DOSE (49643-048-30)
  • ndc11
    4964304850
    50 mL in 1 VIAL, MULTI-DOSE (49643-048-50)

Regulatory notes

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

Same medicine, other countries

Blattella germanica in 1 other country

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

All blattella germanica products

Authorised across Europe · EMA

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

  • Hungary · Alyostal Prick Állati Eredetű Allergének

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/8ca41053-d6f9-4213-8e0b-665816591a90
GET /v1/drugs/8ca41053-d6f9-4213-8e0b-665816591a90?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": ".1",
  "substance": "BLATTELLA GERMANICA",
  "productndc": "49643-048",
  "dosage_form": "INJECTION",
  "dea_schedule": null,
  "strength_unit": "g/mL",
  "application_number": "BLA102211",
  "marketing_category": "BLA"
}

See everything about blattella germanica.

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.