NUROFEN DOUBLE STRENGTH ZAVANCE ibuprofen sodium dihydrate 512 mg sugar coated tablet blister pack

Country: Australia

Language: English

Source: Department of Health (Therapeutic Goods Administration)

Active ingredient:

ibuprofen sodium dihydrate, Quantity: 512 mg

Available from:

Reckitt Benckiser Pty Ltd

INN (International Name):

Ibuprofen sodium dihydrate

Pharmaceutical form:

Tablet, sugar coated

Composition:

Excipient Ingredients: purified talc; Acacia; colloidal anhydrous silica; titanium dioxide; industrial methylated spirit; carmellose sodium; sucrose; microcrystalline cellulose; macrogol 6000; magnesium stearate; croscarmellose sodium; xylitol; purified water; propylene glycol; butan-1-ol; isopropyl alcohol; iron oxide red; strong ammonia solution; simethicone; ethanol; Shellac; sulfuric acid

Administration route:

Oral

Units in package:

50, 48, 24, 12, 6, 2, 4 (samples), 6 (samples)

Prescription type:

(S3) Pharmacist Only Medicine, (S2) Pharmacy Medicine

Therapeutic indications:

Temporary relief of pain (and discomfort) associated with headache, migraine headache, tension headache, sinus pain, toothache, dental procedures, backache, muscular aches and pains, period pain, sore throat, arthritis, rheumatic pain where inflammation is present, and the aches and pains associated with colds and flu. Reduces fever.

Product summary:

Visual Identification: A white to off-white, round, biconvex, sugar coated tablet printed with an identifying logo in red on one face.; Container Type: Blister Pack; Container Material: PVC/PVDC/Al; Container Life Time: 2 Years; Container Temperature: Store below 25 degrees Celsius

Authorization status:

Licence status A

Authorization date:

2014-02-05