United States· US:49281-752_3b4077df-355d-43d9-a762-c74656709f20
TUBERSOL
A medicinal product containing tuberculin purified protein derivative, registered in United States by Sanofi Vaccines US Inc..
Checked against FDA National Drug Code directory (United States) on
Informational only — not a medical device.
The record
At a glance
FDA National Drug Code directory (United States)- Active substance
- TUBERCULIN PURIFIED PROTEIN DERIVATIVE
- Manufacturer
- Sanofi Vaccines US 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 · 4
- ndc1149281-752-21
- ndc1149281-752-22
- ndc1149281752211 VIAL, MULTI-DOSE in 1 CARTON (49281-752-21) / 1 mL in 1 VIAL, MULTI-DOSE (49281-752-78)
- ndc1149281752221 VIAL, MULTI-DOSE in 1 CARTON (49281-752-22) / 5 mL in 1 VIAL, MULTI-DOSE (49281-752-98)
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Tuberculin purified protein derivative in 7 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- BelgiumTuberculin PPD RT23 AJVaccines 10 TU/0,1 mlAJ Vaccines
- FinlandTuberculin PpdStatens Serum Institut
- United KingdomTuberculin PPD RT 23 SSI 100 tuberculin units/ml solution for injection 1.5ml vialsImported (Denmark)
- CzechiaPPD TUBERCULIN MAMMALIAN
- IrelandTuberculin PPD RT23 AJV 2 T.U./0.1 mL, solution for injectionAJ Vaccines A/S
- PolandTuberculin PPD RT23 AJVAJ Vaccines A/S
- CanadaTUBERSOLSANOFI PASTEUR LIMITED
Authorised across Europe · EMA
The same active substance is authorised in 2 EEA countries. Names it is sold under:
- Bulgaria · Ппд Туберкулин Мамалиан
- France · Tubertest
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/e08e5f00-b907-4531-a79c-f23ef4cff5c2 GET /v1/drugs/e08e5f00-b907-4531-a79c-f23ef4cff5c2?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": "INTRADERMAL",
"source": "ndc",
"strength": "5",
"substance": "TUBERCULIN PURIFIED PROTEIN DERIVATIVE",
"productndc": "49281-752",
"dosage_form": "INJECTION, SOLUTION",
"dea_schedule": null,
"strength_unit": "[iU]/.1mL",
"application_number": "BLA103941",
"marketing_category": "BLA"
}See everything about tuberculin purified protein derivative.
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.