Australia - English - Department of Health (Therapeutic Goods Administration)

sanofi-aventis australia pty ltd - sodium aurothiomalate -

Australia - English - Department of Health (Therapeutic Goods Administration)

sanofi-aventis australia pty ltd - sodium aurothiomalate -

Australia - English - Department of Health (Therapeutic Goods Administration)

sanofi-aventis australia pty ltd - sodium aurothiomalate -

Australia - English - Department of Health (Therapeutic Goods Administration)

sodium aurothiomalate -

New Zealand - English - Medsafe (Medicines Safety Authority)

sanofi-aventis new zealand limited - sodium aurothiomalate monohydrate 10mg;   - solution for injection - 10 mg - active: sodium aurothiomalate monohydrate 10mg   excipient: nitrogen phenylmercuric nitrate water for injection

New Zealand - English - Medsafe (Medicines Safety Authority)

sanofi-aventis new zealand limited - sodium aurothiomalate monohydrate 20mg;   - solution for injection - 20 mg - active: sodium aurothiomalate monohydrate 20mg   excipient: nitrogen phenylmercuric nitrate water for injection

New Zealand - English - Medsafe (Medicines Safety Authority)

sanofi-aventis new zealand limited - sodium aurothiomalate monohydrate 50mg;   - solution for injection - 50 mg - active: sodium aurothiomalate monohydrate 50mg   excipient: nitrogen phenylmercuric nitrate water for injection

United Kingdom - English - MHRA (Medicines & Healthcare Products Regulatory Agency)

sanofi - sodium aurothiomalate - solution for injection - 20mg/1ml

United Kingdom - English - MHRA (Medicines & Healthcare Products Regulatory Agency)

sanofi - sodium aurothiomalate - solution for injection - 100mg/1ml

Ireland - English - HPRA (Health Products Regulatory Authority)

may & baker limited - sodium aurothiomalate - solution for injection - 50mg/0.5 millilitre