Ibandronic Acid Sandoz Uniunea Europeană - engleză - EMA (European Medicines Agency)

ibandronic acid sandoz

sandoz gmbh - ibandronic acid - breast neoplasms; neoplasm metastasis; fractures, bone - drugs for treatment of bone diseases, bisphosphonates - ibandronic acid sandoz is indicated for the prevention of skeletal events (pathological fractures, bone complications requiring radiotherapy or surgery) in patients with breast cancer and bone metastases.,

Tray, impression, dental Australia - engleză - Department of Health (Therapeutic Goods Administration)

tray, impression, dental

trade winds global pty ltd t/a rutinident - 16350 - tray, impression, dental - this is a device that is specially designed to contain, support and control the material that is intended to be used in making impressions in the mouth during dental procedures.

DICLOFENAC SODIUM DELAYED RELEASE- diclofenac sodium tablet, delayed release Statele Unite ale Americii - engleză - NLM (National Library of Medicine)

diclofenac sodium delayed release- diclofenac sodium tablet, delayed release

repharm llc - diclofenac sodium (unii: qtg126297q) (diclofenac - unii:144o8ql0l1) - diclofenac sodium 50 mg - carefully consider the potential benefits and risks of diclofenac sodium delayed-release tablets and other treatment options before deciding to use diclofenac. use the lowest effective dose for the shortest duration consistent with individual patient treatment goals ( see warnings; gastrointestinal bleeding, ulceration, and perforation ). diclofenac is indicated: - for relief of the signs and symptoms of osteoarthritis - for relief of the signs and symptoms of rheumatoid arthritis - for acute or long-term use in the relief of signs and symptoms of ankylosing spondylitis diclofenac sodium delayed-release tablets are contraindicated in the following patients: - known hypersensitivity (e.g., anaphylactic reactions and serious skin reactions) to diclofenac or any components of the drug product ( see warnings; anaphylactic reactions, serious skin reacti

MEDICAL GRADE, NITROUS OXIDE Australia - engleză - Department of Health (Therapeutic Goods Administration)

medical grade, nitrous oxide

boc limited - nitrous oxide, quantity: 0.99 l/l - gas, medicinal - excipient ingredients: - indications as at 2 november 2001: nitrous oxide is indicated in adults and children for: 1. general anaesthesia, usually as an adjuvant to other volatile or intravenous anaesthetics. 2. analgesia (with oxygen) eg. dentistry and obstetrics.

Trihexyphenidyl 5mg tablets Regatul Unit - engleză - MHRA (Medicines & Healthcare Products Regulatory Agency)

trihexyphenidyl 5mg tablets

a a h pharmaceuticals ltd - trihexyphenidyl hydrochloride - oral tablet - 5mg

Trihexyphenidyl 5mg tablets Regatul Unit - engleză - MHRA (Medicines & Healthcare Products Regulatory Agency)

trihexyphenidyl 5mg tablets

alliance healthcare (distribution) ltd - trihexyphenidyl hydrochloride - oral tablet - 5mg