胃散

Ülke: Tayvan

Dil: Çince

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

Aktif bileşen:

COPTIS POWDER;;SODIUM BICARBONATE ( EQ TO SODIUM HYDROGEN CARBONATE);;GLYCYRRHIZA RADIX POWDER;;ZINGER POWDER;;ZANTHOXYLUM POWDER;;MAGNESIUM ALUMINUM METASILICATE (NEUSILIN);;CINNAMON POWDER (CINNAMON CORTEX POWDER);;CLOVE POWDER;;FENNEL POWDER (FOENICULI POWDER);;DIASTASE ASPERGILLUS ORYZAE(DIASTASE TAKA);;CALCIUM CARBONATE

Mevcut itibaren:

中國化學製藥股份有限公司 台北巿襄陽路２３號 (03088802)

Farmasötik formu:

散劑

Kompozisyon:

SODIUM BICARBONATE ( EQ TO SODIUM HYDROGEN CARBONATE) (4008000700) 300MG; DIASTASE ASPERGILLUS ORYZAE(DIASTASE TAKA) (4400002100) 100MG; MAGNESIUM ALUMINUM METASILICATE (NEUSILIN) (5604000501) 400MG; CALCIUM CARBONATE (5604001200) (PPT) 200MG; CINNAMON POWDER (CINNAMON CORTEX POWDER) (5610000103) 74.5MG; FENNEL POWDER (FOENICULI POWDER) (5610000301) 20MG; COPTIS POWDER (5612003802) 50MG; CLOVE POWDER (7200000301) 10MG; GLYCYRRHIZA RADIX POWDER (9200004411) 118MG; ZINGER POWDER (9200015001) 24.5MG; ZANTHOXYLUM POWDER (9200016101) 1MG

Paketteki üniteler:

罐裝

Sınıf:

製　劑

Reçete türü:

須經醫師指示使用

Tarafından üretildi:

SANKYO CO. LTD. 173,KOUNOUCHI,NAKAHARA-KAMIJU KU,HIRATSUKA-SHI,KANAGAWA JAPAN. JP

Terapötik endikasyonlar:

食慾不振、胃液分泌過多症、腹部膨脹、消化不良

Ürün özeti:

註銷日期: 1993/12/22; 註銷理由: 移轉（申請商）; 有效日期: 1993/06/30; 英文品名: S.M. POWDER

Yetkilendirme durumu:

已註銷

Yetkilendirme tarihi:

1982-06-30