Depefex XL 150mg capsules Ingilterra - Ingliż - MHRA (Medicines & Healthcare Products Regulatory Agency)

depefex xl 150mg capsules

chiesi ltd - venlafaxine hydrochloride - modified-release capsule - 150mg

Vertab SR 240 tablets Ingilterra - Ingliż - MHRA (Medicines & Healthcare Products Regulatory Agency)

vertab sr 240 tablets

chiesi ltd - verapamil hydrochloride - modified-release tablet - 240mg

SLOMON SR Irlanda - Ingliż - HPRA (Health Products Regulatory Authority)

slomon sr

chiesi limited - isosorbide mononitrate - capsules modified release - 60 milligram

SLOMON SR 60 Milligram Capsules Modified Release Irlanda - Ingliż - HPRA (Health Products Regulatory Authority)

slomon sr 60 milligram capsules modified release

chiesi limited - isosorbide mononitrate - capsules modified release - 60 milligram

Sativex Oromucosal Spray, nabiximols 80 mg/mL pump actuated metered dose aerosol Awstralja - Ingliż - Department of Health (Therapeutic Goods Administration)

sativex oromucosal spray, nabiximols 80 mg/ml pump actuated metered dose aerosol

chiesi australia pty ltd - nabiximols, quantity: 80 mg/ml - spray, solution - excipient ingredients: propylene glycol; peppermint oil; ethanol absolute - sativex is indicated as treatment, for symptom improvement in patients with moderate to severe spasticity due to multiple sclerosis (ms) who have not responded adequately to other anti-spasticity medication and who demonstrate clinically significant improvement in spasticity related symptoms during an initial trial of therapy.

Cleviprex New Zealand - Ingliż - Medsafe (Medicines Safety Authority)

cleviprex

chiesi new zealand limited t/a emerge health - clevidipine 0.5 mg/ml (as clevidipine butyrate);   - emulsion for injection - 0.5 mg/ml - active: clevidipine 0.5 mg/ml (as clevidipine butyrate)   excipient: egg lecithin glycerol sodium hydroxide soya oil water for injection

Curosurf New Zealand - Ingliż - Medsafe (Medicines Safety Authority)

curosurf

chiesi new zealand limited t/a emerge health - poractant alfa 80 mg/ml - suspension for injection - 80 mg/ml - active: poractant alfa 80 mg/ml excipient: sodium bicarbonate sodium chloride - ·treatment of respiratory distress syndrome (rds) in pre-term babies. ·prophylactic use in premature infants at risk for rds.

ASACOL mesalazine 800 mg enteric coated tablets blister pack Awstralja - Ingliż - Department of Health (Therapeutic Goods Administration)

asacol mesalazine 800 mg enteric coated tablets blister pack

chiesi australia pty ltd - mesalazine, quantity: 800 mg - tablet, enteric coated - excipient ingredients: lactose monohydrate; sodium starch glycollate type a; magnesium stearate; purified talc; povidone; methacrylic acid copolymer; triethyl citrate; iron oxide yellow; iron oxide red; macrogol 6000 - for the treatment of mild to moderate ulcerative colitis and maintenance of remission in adults.