培芬隆滴劑

Šalis: Taivanas

kalba: kinų

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

Veiklioji medžiaga:

SILIOUS EARTH;;CALCIUM CARBONATE;;FERRIC IODATE;;PULSATILLE;;FERRIC AMMONIUM CITRATE;;THIAMINE HYDROCHLORIDE;;POTASSIUM PHOSPHATE ( eq to POTASSIUM PHOSPHATE DIBASIC);;COPPER ACETATE;;SULFUR;;DEXTROSE MONOHYDRATE;;VALERIANA OFFICINALIS

Prieinama:

達星貿易股份有限公司 台北巿仁愛路二段３４號６Ｆ之１ (04205096)

Vaisto forma:

滴劑

Sudėtis:

FERRIC AMMONIUM CITRATE (2004400100) 100MG; FERRIC IODATE (2004402300) D4 (0.01%W/V) 10MG; VALERIANA OFFICINALIS (2824000620) (D3) (0.1%W/V) 5MG; DEXTROSE MONOHYDRATE (4020000570) 100MG; CALCIUM CARBONATE (5604001200) *PPT(0.001%W/V)5MG; POTASSIUM PHOSPHATE ( eq to POTASSIUM PHOSPHATE DIBASIC) (5612001900) D11 (1**-9%W/V)5MG; SULFUR (8428000900) *PPT(1**-9%W/V)5MG; THIAMINE HYDROCHLORIDE (8810100900) 0.3MG; COPPER ACETATE (9200013400) D11 (1**-9%W/V)5MG; PULSATILLE (9200013500) (D4)(0.01%W/V)25MG; SILIOUS EARTH (9600043000) 5MG

Vienetai pakuotėje:

瓶裝

Klasė:

製　劑

Recepto tipas:

須由醫師處方使用

Pagaminta:

JULIUS REDEL CESRA-ARZNEIMITTEL FABRIK GMBH & CO. 7570 BADEN-BADEN P.O. BOX 740 DE

Terapinės indikacijos:

缺鐵性貧血

Produkto santrauka:

註銷日期: 1993/04/15; 註銷理由: 有效期間已屆未能補件; 有效日期: 1994/07/31; 英文品名: PRAEFEMINON

Autorizacija statusas:

已註銷

Leidimo data:

1981-07-31