PREGABALIN SANDOZ pregabalin 25mg capsule blister pack 澳大利亚 - 英文 - Department of Health (Therapeutic Goods Administration)

pregabalin sandoz pregabalin 25mg capsule blister pack

sandoz pty ltd - pregabalin, quantity: 25 mg - capsule - excipient ingredients: iron oxide red; iron oxide yellow; titanium dioxide; gelatin; iron oxide black; maize starch; pregelatinised maize starch; purified talc - pregabalin sandoz is indicated for the treatment of neuropathic pain in adults. pregabalin sandoz is indicated as adjunctive therapy in adults with partial seizures with or without secondary generalisation.

PREGABALIN SANDOZ pregabalin 150mg capsule blister pack 澳大利亚 - 英文 - Department of Health (Therapeutic Goods Administration)

pregabalin sandoz pregabalin 150mg capsule blister pack

sandoz pty ltd - pregabalin, quantity: 150 mg - capsule - excipient ingredients: maize starch; gelatin; titanium dioxide; pregelatinised maize starch; purified talc - pregabalin sandoz is indicated for the treatment of neuropathic pain in adults. pregabalin sandoz is indicated as adjunctive therapy in adults with partial seizures with or without secondary generalisation.

PREGABALIN SANDOZ pregabalin 75mg capsule blister pack 澳大利亚 - 英文 - Department of Health (Therapeutic Goods Administration)

pregabalin sandoz pregabalin 75mg capsule blister pack

sandoz pty ltd - pregabalin, quantity: 75 mg - capsule - excipient ingredients: pregelatinised maize starch; iron oxide red; gelatin; titanium dioxide; purified talc; iron oxide yellow; maize starch - pregabalin sandoz is indicated for the treatment of neuropathic pain in adults. pregabalin sandoz is indicated as adjunctive therapy in adults with partial seizures with or without secondary generalisation.

Capecitabine Sandoz capecitabine 500mg film coated tablet blister pack 澳大利亚 - 英文 - Department of Health (Therapeutic Goods Administration)

capecitabine sandoz capecitabine 500mg film coated tablet blister pack

sandoz pty ltd - capecitabine, quantity: 500 mg - tablet, film coated - excipient ingredients: titanium dioxide; iron oxide red; lactose monohydrate; magnesium stearate; hypromellose; microcrystalline cellulose; purified talc; croscarmellose sodium - colon cancer,capecitabine sandoz is indicated for the adjuvant treatment of patients with dukes' stage c and high-risk stage b, colon cancer, either as monotherapy or in combination with oxaliplatin.,colorectal cancer,capecitabine sandoz is indicated for the treatment of patients with advanced or metastatic colorectal cancer.,oesophagogastric cancer,capecitabine sandoz is indicated for the first-line treatment of patients with advanced oesophagogastric cancer in combination with a platinum-based regimen.,breast cancer,capecitabine sandoz is indicated for the treatment of patients with locally advanced or metastatic breast cancer after failure of taxanes and an anthracycline containing chemotherapy regimen unless therapy with these and other standard agents are clinically contraindicated.,capecitabine sandoz in combination with docetaxel is indicated for the treatment of patients with locally advanced or metastatic breast cancer after failure of prior anthracycline containing chemotherapy.

Capecitabine Sandoz capecitabine 150mg film coated tablet blister pack 澳大利亚 - 英文 - Department of Health (Therapeutic Goods Administration)

capecitabine sandoz capecitabine 150mg film coated tablet blister pack

sandoz pty ltd - capecitabine, quantity: 150 mg - tablet, film coated - excipient ingredients: lactose monohydrate; microcrystalline cellulose; hypromellose; croscarmellose sodium; titanium dioxide; purified talc; magnesium stearate; iron oxide red - colon cancer,capecitabine sandoz is indicated for the adjuvant treatment of patients with dukes' stage c and high-risk stage b, colon cancer, either as monotherapy or in combination with oxaliplatin.,colorectal cancer,capecitabine sandoz is indicated for the treatment of patients with advanced or metastatic colorectal cancer.,oesophagogastric cancer,capecitabine sandoz is indicated for the first-line treatment of patients with advanced oesophagogastric cancer in combination with a platinum-based regimen.,breast cancer,capecitabine sandoz is indicated for the treatment of patients with locally advanced or metastatic breast cancer after failure of taxanes and an anthracycline containing chemotherapy regimen unless therapy with these and other standard agents are clinically contraindicated.,capecitabine sandoz in combination with docetaxel is indicated for the treatment of patients with locally advanced or metastatic breast cancer after failure of prior anthracycline containing chemotherapy.

TELMISARTAN/HCT SANDOZ 80mg/12.5mg telmisartan 80mg / hydrochlorothiazide 12.5mg blister pack 澳大利亚 - 英文 - Department of Health (Therapeutic Goods Administration)

telmisartan/hct sandoz 80mg/12.5mg telmisartan 80mg / hydrochlorothiazide 12.5mg blister pack

sandoz pty ltd - telmisartan, quantity: 80 mg; hydrochlorothiazide, quantity: 12.5 mg - tablet, film coated - excipient ingredients: lactose; povidone; citric acid monohydrate; sodium hydroxide; macrogol poly(vinyl alcohol) grafted polymer; magnesium stearate; meglumine; colloidal anhydrous silica; lactose monohydrate; crospovidone - telmisartan/hct sandoz? is indicated for the treatment of hypertension. treatment should not be initiated with these combinations.

TELMISARTAN/HCT SANDOZ 80mg/25mg telmisartan 80mg / hydrochlorothiazide 25mg blister pack 澳大利亚 - 英文 - Department of Health (Therapeutic Goods Administration)

telmisartan/hct sandoz 80mg/25mg telmisartan 80mg / hydrochlorothiazide 25mg blister pack

sandoz pty ltd - hydrochlorothiazide, quantity: 25 mg; telmisartan, quantity: 80 mg - tablet, film coated - excipient ingredients: meglumine; sodium hydroxide; citric acid monohydrate; lactose; macrogol poly(vinyl alcohol) grafted polymer; povidone; magnesium stearate; colloidal anhydrous silica; iron oxide yellow; lactose monohydrate; crospovidone - telmisartan/hct sandoz? is indicated for the treatment of hypertension. treatment should not be initiated with these combinations.

TELMISARTAN/HCT SANDOZ  40mg/12.5mg telmisartan 40mg / hydrochlorothiazide 12.5mg blister pack 澳大利亚 - 英文 - Department of Health (Therapeutic Goods Administration)

telmisartan/hct sandoz 40mg/12.5mg telmisartan 40mg / hydrochlorothiazide 12.5mg blister pack

sandoz pty ltd - hydrochlorothiazide, quantity: 12.5 mg; telmisartan, quantity: 40 mg - tablet, film coated - excipient ingredients: iron oxide red; povidone; meglumine; magnesium stearate; sodium hydroxide; lactose; iron oxide yellow; macrogol poly(vinyl alcohol) grafted polymer; citric acid monohydrate; colloidal anhydrous silica; lactose monohydrate; crospovidone - telmisartan/hct sandoz? is indicated for the treatment of hypertension. treatment should not be initiated with these combinations.

SANDOZ ANUZINC HC OINTMENT 加拿大 - 英文 - Health Canada

sandoz anuzinc hc ointment

sandoz canada incorporated - zinc sulfate; hydrocortisone acetate - ointment - 5mg; 5mg - zinc sulfate 5mg; hydrocortisone acetate 5mg - anti-inflammatory agents

DOCETAXEL SANDOZ 澳大利亚 - 英文 - Department of Health (Therapeutic Goods Administration)

docetaxel sandoz

sandoz pty ltd - docetaxel, quantity: 80 mg - injection, concentrated - excipient ingredients: ethanol; polysorbate 80; citric acid; nitrogen - docetaxel sandoz is indicated for the treatment of patients with locally advanced or metastatic breast cancer in whom previous chemotherapy has failed. docetaxel sandoz in combination with capecitabine is indicated for the treatment of patients with locally advanced or metastatic breast cancer after failure of prior anthracycline containing chemotherapy. docetaxel sandoz in combination with trastuzumab is indicated for the treatment of patients with metastatic breast cancer whose tumours overexpress her2 and who previously have not received chemotherapy for metastatic disease. docetaxel sandoz in combination with doxorubicin and cyclophosphamide is indicated for the adjuvant treatment of patients with node-positive breast cancer. doxorubicin and cyclophosphamide followed by docetaxel sandoz in combination with trastuzumab (ac-th) is indicated for the adjuvant treatment of patients with operable breast cancer whose tumours overexpress her2. docetaxel sandoz in combination with carboplatin and trastuzumab (tch) is indicated for the adjuvant treatment of patients with operable breast cancer whose tumours overexpress her2. docetaxel in combination with cyclophosphamide is indicated for the adjuvant treatment of operable breast cancer with a primary tumour of =1cm and < 7cm. docetaxel sandoz is indicated for the treatment of patients with locally advanced or metastatic non small cell lung cancer, including those who have failed platinum-based chemotherapy. docetaxel sandoz is indicated for the treatment of metastatic carcinoma of the ovary after failure of firstline or subsequent chemotherapy. docetaxel sandoz is indicated for the treatment of patients with androgen independent (hormone refractory) prostate cancer. docetaxel sandoz, in combination with cisplatin and fluorouracil is indicated as induction treatment prior to chemoradiotherapy, for the treatment of patients with locally advanced, squamous cell carcinoma of the head and neck, who have low probability of surgical cure, require organ preservation or where the tumour is technically unresectable.