Prexige

Country: New Zealand

Bahasa: Inggeris

Sumber: Medsafe (Medicines Safety Authority)

Bahan aktif:

Lumiracoxib 200mg (release testing to occur at Novartis AG, Lichstrasse, Basel.)

Boleh didapati daripada:

Novartis New Zealand Ltd

INN (Nama Antarabangsa):

Lumiracoxib 200 mg (release testing to occur at Novartis AG, Lichstrasse, Basel.)

Dos:

200 mg

Borang farmaseutikal:

Film coated tablet

Komposisi:

Active: Lumiracoxib 200mg (release testing to occur at Novartis AG, Lichstrasse, Basel.) Excipient: Croscarmellose sodium Lactose monohydrate Magnesium stearate Microcrystalline cellulose Opadry black 00F17713 Opadry red 00F15613 Opadry white 00F18296 Povidone Titanium dioxide

Unit dalam pakej:

Blister pack, PVC/Al x 2 tablets, 2 tablets

Kelas:

Prescription

Jenis preskripsi:

Prescription

Dikeluarkan oleh:

Novartis Grimsby Limited

Ringkasan produk:

Package - Contents - Shelf Life: Blister pack, PVC/Al x 2 tablets - 2 tablets - 36 months from date of manufacture stored at or below 30°C - Blister pack, PVC/Al x 10 tablets - 10 tablets - 36 months from date of manufacture stored at or below 30°C - Blister pack, PVC/Al x 20 tablets - 20 tablets - 36 months from date of manufacture stored at or below 30°C - Blister pack, PVC/Al x 30 tablets - 30 tablets - 36 months from date of manufacture stored at or below 30°C - Blister pack, PVC/Al x 50 tablets - 50 tablets - 36 months from date of manufacture stored at or below 30°C - Blister pack, PVC/Al x 100 tablets - 100 tablets - 36 months from date of manufacture stored at or below 30°C

Tarikh kebenaran:

2003-01-09