多力蘇

Country: Tajwan

Lingwa: Ċiniż

Sors: 衛生福利部食品藥物管理署 (Ministry of Health and Welfare, Food And Drug Administration)

Ingredjent attiv:

DEXTROSE;;SODIUM CHLORIDE;;POTASSIUM CHLORIDE;;CALCIUM CHLORIDE;;MAGNESIUM CHLORIDE HEXAHYDRATE (EQ TO MAGNESIUM CHLORIDE 6H2O);;SODIUM LACTATE;;SODIUM ACETATE;;SODIUM BISULFITE (EQ TO SODIUM HYDROGEN SULFITE)

Disponibbli minn:

天行貿易股份有限公司 台北巿長安東路一段36號7樓703室 (11102308)

Għamla farmaċewtika:

透析用液劑

Kompożizzjoni:

SODIUM ACETATE (4008000600) 163MG; SODIUM LACTATE (4008000900) 134MG; CALCIUM CHLORIDE (4012000300) 36.8MG; MAGNESIUM CHLORIDE HEXAHYDRATE (EQ TO MAGNESIUM CHLORIDE 6H2O) (4012001550) 30.5MG; POTASSIUM CHLORIDE (4012001800) 119.0MG; SODIUM CHLORIDE (4012002100) 93.5MG; DEXTROSE (4020000500) 5.0GM; SODIUM BISULFITE (EQ TO SODIUM HYDROGEN SULFITE) (6400000600) 16.2MG

Unitajiet fil-pakkett:

瓶裝

Klassi:

製 劑

Tip ta 'preskrizzjoni:

限由醫師使用

Manifatturat minn:

BAYER CORPORATION 800 DWIGHT WAY P.O. BOX 1986 BERKELEY, CA 94701-1986, U.S.A. US

Indikazzjonijiet terapewtiċi:

內外小兒各科病人不能以口攝取食物、注射本劑以補充營養

Sommarju tal-prodott:

註銷日期: 1986/04/30; 註銷理由: 有效期間已屆未能補件; 有效日期: 1985/07/14; 英文品名: POLYSAL "M"

L-istatus ta 'awtorizzazzjoni:

已註銷

Data ta 'l-awtorizzazzjoni:

1970-07-14

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