Suurbritannia - inglise - MHRA (Medicines & Healthcare Products Regulatory Agency)

bayer plc - ciprofloxacin hydrochloride - oral tablet - 750mg

Suurbritannia - inglise - MHRA (Medicines & Healthcare Products Regulatory Agency)

bayer plc - ciprofloxacin hydrochloride - oral tablet - 500mg

Uus-Meremaa - inglise - Medsafe (Medicines Safety Authority)

rex medical ltd - ciprofloxacin hydrochloride 291.08mg equivalent to ciprofloxacin base 250 mg;   - film coated tablet - 250 mg - active: ciprofloxacin hydrochloride 291.08mg equivalent to ciprofloxacin base 250 mg   excipient: colloidal silicon dioxide croscarmellose sodium hypromellose purified talc croscarmellose sodium macrogol 6000 magnesium stearate microcrystalline cellulose povidone propylene glycol purified talc titanium dioxide

Uus-Meremaa - inglise - Medsafe (Medicines Safety Authority)

rex medical ltd - ciprofloxacin hydrochloride 582.16mg equivalent to ciprofloxacin base 500 mg;   - film coated tablet - 500 mg - active: ciprofloxacin hydrochloride 582.16mg equivalent to ciprofloxacin base 500 mg   excipient: colloidal silicon dioxide croscarmellose sodium hypromellose purified talc croscarmellose sodium macrogol 6000 magnesium stearate microcrystalline cellulose povidone propylene glycol purified talc titanium dioxide

Uus-Meremaa - inglise - Medsafe (Medicines Safety Authority)

rex medical ltd - ciprofloxacin hydrochloride 873.24mg equivalent to ciprofloxacin base 750 mg;   - film coated tablet - 750 mg - active: ciprofloxacin hydrochloride 873.24mg equivalent to ciprofloxacin base 750 mg   excipient: colloidal silicon dioxide croscarmellose sodium hypromellose purified talc croscarmellose sodium macrogol 6000 magnesium stearate microcrystalline cellulose povidone propylene glycol purified talc titanium dioxide

Austraalia - inglise - Department of Health (Therapeutic Goods Administration)

novartis pharmaceuticals australia pty ltd - ciprofloxacin, quantity: 2 mg/ml; hydrocortisone, quantity: 10 mg/ml - ear drops, suspension - excipient ingredients: polysorbate 20; sodium acetate; glacial acetic acid; benzyl alcohol; hydrogenated soy phosphatidylcholine; sodium chloride; polyvinyl alcohol; purified water - for the treatment of acute bacterial otitis externa, caused by organisms susceptible to ciprofloxacin (see pharmacology), in adults and children aged 2 years and older.

Austraalia - inglise - Department of Health (Therapeutic Goods Administration)

alcon laboratories australia pty ltd - hydrocortisone; ciprofloxacin -

Austraalia - inglise - Department of Health (Therapeutic Goods Administration)

bayer australia ltd - ciprofloxacin -

Austraalia - inglise - Department of Health (Therapeutic Goods Administration)

bayer australia ltd - ciprofloxacin -

Ameerika Ühendriigid - inglise - NLM (National Library of Medicine)

unifirst first aid corporation - naproxen sodium (unii: 9tn87s3a3c) (naproxen - unii:57y76r9atq) - purpose pain reliever/fever reducer uses temporarily relieves minor aches and pains due to - minor pain of arthritis - muscular aches - backache - menstrual cramps - headache - toothache - the common cold temporarily reduces fever stop use and ask a doctor if ■ you experience any of the following signs of stomach bleeding: ■ feel faint ■ vomit blood ■ have bloody or black stools ■ have stomach pain that does not get better ■ you have symptoms of heart problems or stroke: ■ chest pain ■ trouble breathing ■ weakness in one part or side of body ■ slurred speech ■ leg swelling ■ pain gets worse or lasts for more than 10 days ■ fever gets worse or lasts for more than 3 days ■ you have difficulty swallowing ■ it feels like the pill is stuck in your throat ■ redness or swelling is present in the painful area ■ any new symptoms appear