innohep 18,000 IU in 0.9 ml, solution for injection Ireland - English - HPRA (Health Products Regulatory Authority)

innohep 18,000 iu in 0.9 ml, solution for injection

leo laboratories limited - tinzaparin sodium - solution for injection - 18,000 iu in 0.9 ml international unit(s)/millilitre - heparin group; tinzaparin

Spiriva 18 microgram inhalation powder, hard capsule Ireland - English - HPRA (Health Products Regulatory Authority)

spiriva 18 microgram inhalation powder, hard capsule

imed healthcare ltd. - tiotropium - inhalation powder, hard capsule - 18 microgram(s) - anticholinergics; tiotropium bromide

Spiriva 18 microgram inhalation powder, hard capsule Ireland - English - HPRA (Health Products Regulatory Authority)

spiriva 18 microgram inhalation powder, hard capsule

pco manufacturing ltd. - tiotropium - inhalation powder, hard capsule - 18 microgram(s) - anticholinergics; tiotropium bromide

Spiriva 18 microgram, inhalation powder, hard capsule Ireland - English - HPRA (Health Products Regulatory Authority)

spiriva 18 microgram, inhalation powder, hard capsule

imbat limited - tiotropium bromide - inhalation powder, hard capsule - 18 microgram(s) - anticholinergics; tiotropium bromide

Srivasso 18 microgram, inhalation powder, hard capsule Ireland - English - HPRA (Health Products Regulatory Authority)

srivasso 18 microgram, inhalation powder, hard capsule

boehringer ingelheim international gmbh - tiotropium - inhalation powder, hard capsule - 18 microgram(s) - anticholinergics; tiotropium bromide

Ceporex 18 %w/v Suspension for Injection Ireland - English - HPRA (Health Products Regulatory Authority)

ceporex 18 %w/v suspension for injection

intervet ireland limited - cefalexin sodium - suspension for injection - 18 percent weight/volume - cefalexin - cattle, dogs, cats - antibacterial

Panacur Equine Oral Paste 18.75 %w/w Ireland - English - HPRA (Health Products Regulatory Authority)

panacur equine oral paste 18.75 %w/w

intervet ireland limited - fenbendazole - oral paste - 18.75 percent weight/weight - fenbendazole - horses - endoparasiticide

LECTEVA levodopa/carbidopa/entacapone 75 mg/18.75 mg/200 mg tablet bottle Australia - English - Department of Health (Therapeutic Goods Administration)

lecteva levodopa/carbidopa/entacapone 75 mg/18.75 mg/200 mg tablet bottle

teva pharma australia pty ltd - levodopa, quantity: 75 mg; carbidopa monohydrate, quantity: 20.25 mg (equivalent: carbidopa, qty 18.75 mg); entacapone, quantity: 200 mg - tablet, film coated - excipient ingredients: microcrystalline cellulose; lactose; hyprolose; povidone; colloidal anhydrous silica; magnesium stearate; hypromellose; titanium dioxide; glycerol; iron oxide yellow; polysorbate 80; iron oxide red - lecteva (levodopa/carbidopa/entacapone) is indicated for the management of patients with parkinson?s disease who are experiencing motor fluctuations.

CY BETTER LIPS BALM HUMECTANTE PARA LABIOS CON COLOR FPS 18 (BLUSH CURE) - PINK- avobenzone, octisalate, zinc oxide, octinoxate, United States - English - NLM (National Library of Medicine)

cy better lips balm humectante para labios con color fps 18 (blush cure) - pink- avobenzone, octisalate, zinc oxide, octinoxate,

ventura corporation ltd - avobenzone (unii: g63qqf2nox) (avobenzone - unii:g63qqf2nox), octisalate (unii: 4x49y0596w) (octisalate - unii:4x49y0596w), zinc oxide (unii: soi2loh54z) (zinc oxide - unii:soi2loh54z), octinoxate (unii: 4y5p7mud51) (octinoxate - unii:4y5p7mud51), oxybenzone (unii: 95oos7ve0y) (oxybenzone - unii:95oos7ve0y) - avobenzone 0.0003 g in 1 g

AXUMIN- fluciclovine f-18 injection, solution United States - English - NLM (National Library of Medicine)

axumin- fluciclovine f-18 injection, solution

blue earth diagnostics - fluciclovine f-18 (unii: 38r1q0l1ze) (fluciclovine f-18 - unii:38r1q0l1ze) - fluciclovine f-18 221 mci in 1 ml - axumin is indicated for positron emission tomography (pet) in men with suspected prostate cancer recurrence based on elevated blood prostate specific antigen (psa) levels following prior treatment. none risk summary axumin is not indicated for use in females and there is no information on the risk of adverse development outcomes in pregnant women or animals with the use of fluciclovine f 18. risk summary axumin is not indicated for use in females and there is no information of the presence of fluciclovine f 18 in human milk. safety and effectiveness have not been established in pediatric patients. of the total number of patients in clinical studies of axumin, the average age was 66 years with a range of 21 to 90 years. no overall differences in safety or effectiveness were observed between older subjects and younger subjects.