Belgium - English - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

bimeda animal health ltd. - ivermectin 18,7 mg/g - oral paste - 18,7 mg/g - ivermectin 18.7 mg/g - ivermectin - horse

Belgium - English - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

eco animal health europe ltd. - ivermectin 18,7 mg/g - oral paste - 18,7 mg/g - ivermectin 18.7 mg/g - ivermectin - horse

Belgium - English - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

norbrook laboratories (ireland) ltd. - ivermectin 18,7 mg/g - oral paste - 18,7 mg/g - ivermectin 18.7 mg/g - ivermectin - horse

Belgium - English - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

norbrook laboratories (ireland) ltd. - praziquantel 140,3 mg/g; ivermectin 18,7 mg/g - oral paste - 18,7 mg/g - 140,3 mg/g - ivermectin 18.7 mg/g; praziquantel 140.3 mg/g - ivermectin, combinations - horse

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

quality care products, llc - tramadol hydrochloride (unii: 9n7r477wck) (tramadol - unii:39j1lgj30j) - tramadol hydrochloride tablets, usp are indicated in adults for the management of pain severe enough to require an opioid analgesic and for which alternative treatments are inadequate. limitations of use because of the risks of addiction, abuse, and misuse with opioids, even at recommended doses [see warnings and precautions (5.1)] , reserve tramadol hydrochloride tablets for use in patients for whom alternative treatment options [e.g., non-opioid analgesics]: - have not been tolerated or are not expected to be tolerated. - have not provided adequate analgesia or are not expected to provide adequate analgesia. tramadol hydrochloride tablets, usp are contraindicated for: -   all children younger than 12 years of age [ see warnings and precautions (5.4) ]. -   post-operative management in children younger than 18 years of age following tonsillectomy and/or adenoidectomy

Panama - English - Ministerio de Salud (Dirección Nacional de Farmacia Y Drogas)

radiofarmacia de centroamerica s.a - fluodeoxiglucosa 18 f - fluodeoxiglucosa 18 f....15 mci/0.55 gbq a 3ci/111 gbq en 3 ml a 19 ml

New Zealand - English - Medsafe (Medicines Safety Authority)

roche products (nz) ltd - interferon alfa-2a 18 miu - powder for injection - 18 miu - active: interferon alfa-2a 18 miu excipient: albumin sodium chloride water for injection

New Zealand - English - Medsafe (Medicines Safety Authority)

orion pharma (nz) limited - carbidopa monohydrate 20.25mg equivalent to 18.75 mg carbidopa; entacapone 200mg; levodopa 75mg - film coated tablet - 75mg/18.75mg/200mg - active: carbidopa monohydrate 20.25mg equivalent to 18.75 mg carbidopa entacapone 200mg levodopa 75mg excipient: croscarmellose sodium ethanol glycerol hypromellose iron oxide red magnesium stearate   maize starch mannitol polysorbate 80 povidone purified water sucrose titanium dioxide - stalevo is indicated for the treatment of patients with parkinson's disease and end-of-dose motor fluctuations not stabilised on levodopa/dopa decarboxylase (ddc) inhibitor treatment.

Ireland - English - HPRA (Health Products Regulatory Authority)

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

Ireland - English - HPRA (Health Products Regulatory Authority)

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