Singapūra - angļu - HSA (Health Sciences Authority)

novartis (singapore) pte ltd - diclofenac sodium - suppository - 25 mg - diclofenac sodium 25 mg

Singapūra - angļu - HSA (Health Sciences Authority)

novartis (singapore) pte ltd - diclofenac sodium - suppository - 50 mg - diclofenac sodium 50 mg

Malta - angļu - Medicines Authority

novartis pharmaceuticals uk limited - diclofenac sodium 100 mg - suppository

Saūda Arābija - angļu - SFDA (Saudi Food and Drug Authority)- الهيئة العامة للغذاء والدواء

novartis - diclofenac sodium - suppository - 100 mg

Austrālija - angļu - Department of Health (Therapeutic Goods Administration)

novartis pharmaceuticals australia pty ltd - diclofenac sodium, quantity: 12.5 mg - suppository, moulded - excipient ingredients: hydrogenated coco-glycerides; hard fat - inflammatory and degenerative forms of rheumatism: rheumatoid arthritis and osteoarthritis. short term (up to three days) treatment of post-operative pain in children.

Ēģipte - angļu - EDA (Egyptian Drug Authority)

novartis pharma-switzerland - suppository - 100 mg

Singapūra - angļu - HSA (Health Sciences Authority)

novartis (singapore) pte ltd - diclofenac sodium - suppository - 12.5 mg - diclofenac sodium 12.5 mg

Namībija - angļu - Namibia Medicines Regulatory Council

novartis south africa (pty) ltd - diclofenac sodium - suppository - 100 mg/suppository

Kanāda - angļu - Health Canada

teva canada limited - diclofenac sodium - suppository - 100mg - diclofenac sodium 100mg - other nonsteroidal antiimflammatory agents

Lielbritānija - angļu - MHRA (Medicines & Healthcare Products Regulatory Agency)

novartis pharmaceuticals uk ltd - diclofenac sodium - suppository - 100mg