MedPath
HSA Product

TUBERCULIN PPD RT 23 AJV

Product approved by Health Sciences Authority (SG)

Basic Information

TUBERCULIN PPD RT 23 AJV

INJECTION

Regulatory Information

SIN09944P

August 19, 1998

Prescription Only

Therapeutic

SUBCUTANEOUS

August 10, 2023

June 4, 2025

XV04CF01

Company Information

AJ Vaccines A/S

AJ BIOLOGICS PTE. LTD.

DKSH SINGAPORE PTE. LTD.

Active Ingredients

TUBERCULIN PPD RT 23

Strength: 0.4 mcg/ml

Detailed Information

Contraindications

**2.3 Contraindications** Tuberculin PPD RT 23 AJV should not be administered to: - Individuals known to be hypersensitive (Type I) to the active substance or any of the excipients of the medicinal product listed in section 1 – _please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information_. - Individuals who previously have experienced a severe local reaction to tuberculin products. A severe local reaction may include vesicles and ulceration at the injection site and skin necrosis at the centre of a widespread tuberculin reaction. The necrosis will generally disappear after a few days.

Indication Information

**2.1 Therapeutic indications** Tuberculin PPD RT 23 AJV is used for Mantoux tuberculin skin testing to diagnose if an individual has ever been infected with _Mycobacterium tuberculosis_. Some countries also recommend Mantoux tuberculin skin testing in conjunction with BCG vaccination, either to ensure that only tuberculin-negative individuals are vaccinated or as a post-vaccination test. Tuberculin PPD RT 23 AJV can be used in all age groups. This medicinal product is for diagnostic use only.

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