DESLORELIN powder United States - English - NLM (National Library of Medicine)

deslorelin powder

professional compounding centers of america - deslorelin (unii: tkg3i66tve) (deslorelin - unii:tkg3i66tve) - deslorelin acetate (for veterinary use) for veterinary use only. part: 30-5206 gm cas: 82318-06-7 danger: may be harmful if swallowed. may cause damage to fertility or unborn child. may cause eye irritation. may cause mild skin irritation. store in tightly closed container. store in a freezer.

DESLORATADINE tablet, film coated United States - English - NLM (National Library of Medicine)

desloratadine tablet, film coated

bionpharma inc. - desloratadine (unii: fvf865388r) (desloratadine - unii:fvf865388r) - desloratadine tablets are indicated for the relief of the nasal and non-nasal symptoms of seasonal allergic rhinitis in patients 12 years of age and older. desloratadine tablets are indicated for the relief of the nasal and non-nasal symptoms of perennial allergic rhinitis in patients 12 years of age and older. desloratadine tablets are indicated for the symptomatic relief of pruritus, reduction in the number of hives, and size of hives, in patients with chronic idiopathic urticaria 12 years of age and older. desloratadine tablets are contraindicated in patients who are hypersensitive to this medication or to any of its ingredients or to loratadine [see warnings and precautions (5.1) and adverse reactions ( 6.2)]. risk summary the limited available data with desloratadine in pregnant women are not sufficient to inform a drug-associated risk for major birth defects and miscarriage. there are no adequate and well-controlled studies in pregnant women. desloratadine given during organogenesis to pregnant rats was

Deslor New Zealand - English - Medsafe (Medicines Safety Authority)

deslor

multichem nz limited - desloratadine 5mg - film coated tablet - 5 mg - active: desloratadine 5mg excipient: colloidal silicon dioxide hydrogenated castor oil hyprolose mannitol 25 mannitol opadry blue 04f50656 purified talc purified water

SUCROMATE EQUINE DESLORELIN ACETATE STERILE SUSPENSION Australia - English - APVMA (Australian Pesticides and Veterinary Medicines Authority)

sucromate equine deslorelin acetate sterile suspension

thorn bioscience llc (a division of creosalus inc.) - deslorelin as deslorelin acetate - parenteral liquid/solution/suspension - deslorelin as deslorelin acetate ungrouped active 1.7 mg/ml - endocrine system

SUPRELORIN F- deslorelin acetate implant United States - English - NLM (National Library of Medicine)

suprelorin f- deslorelin acetate implant

virbac ah, inc. - deslorelin acetate (unii: 679007nr5c) (deslorelin - unii:tkg3i66tve) - deslorelin acetate 4.7 mg - suprelorin® f (4.7 mg) implant is indicated for the management of adrenal gland cortical disease in the male and female domestic ferret. do not use this product in ferrets with known hypersensitivity to deslorelin acetate or other synthetic hormones.

CLARINEX- desloratadine tablet, film coated United States - English - NLM (National Library of Medicine)

clarinex- desloratadine tablet, film coated

rebel distributors corp - desloratadine (unii: fvf865388r) (desloratadine - unii:fvf865388r) - desloratadine 5 mg - clarinex is indicated for the relief of the nasal and non-nasal symptoms of seasonal allergic rhinitis in patients 2 years of age and older. clarinex is indicated for the relief of the nasal and non-nasal symptoms of perennial allergic rhinitis in patients 6 months of age and older. clarinex is indicated for the symptomatic relief of pruritus, reduction in the number of hives, and size of hives, in patients with chronic idiopathic urticaria 6 months of age and older. clarinex tablets 5 mg are contraindicated in patients who are hypersensitive to this medication or to any of its ingredients, or to loratadine. there is no information to indicate that abuse or dependency occurs with clarinex tablets.

CHEMISTS' OWN DESLORATADINE HAYFEVER & ALLERGY RELIEF desloratadine 5 mg tablet blister pack Australia - English - Department of Health (Therapeutic Goods Administration)

chemists' own desloratadine hayfever & allergy relief desloratadine 5 mg tablet blister pack

arrotex pharmaceuticals pty ltd - desloratadine, quantity: 5 mg - tablet, film coated - excipient ingredients: lactose monohydrate; pregelatinised starch; microcrystalline cellulose; magnesium stearate; colloidal anhydrous silica; hydrogenated cottonseed oil; dibasic sodium phosphate; maize starch; titanium dioxide; purified talc; xanthan gum; polyvinyl alcohol; lecithin; indigo carmine aluminium lake - the rapid relief of symptoms associated with seasonal allergic rhinitis. the nasal symptoms of allergic rhinits include rhinorrhoea, sneezing and nasal itching. allergic rhinitis is also associated with non-nasal symptoms such as ocular itching, tearing and itching of the eyes or palate. the relief of symptoms associated with perennial allergic rhinitis. the symptomatic relief of itching and reduction in the size and number of hives associated with chronic idiopathic urticaria.

Desloratadine 0.5 mg/ml oral solution Ireland - English - HPRA (Health Products Regulatory Authority)

desloratadine 0.5 mg/ml oral solution

accord healthcare ireland ltd. - desloratidine - oral solution - 0.5 milligram(s)/millilitre - other antihistamines for systemic use; desloratadine

Deslor 0.5 mg/ml Oral Solution Ireland - English - HPRA (Health Products Regulatory Authority)

deslor 0.5 mg/ml oral solution

rowex ltd - desloratidine - oral solution - 0.5 milligram(s)/millilitre - other antihistamines for systemic use; desloratadine

Deslora Namibia - English - Namibia Medicines Regulatory Council

deslora

cipla - medpro (pty) ltd - desloratadine - tablet - each tablet contains desloratadine 5,0 mg