太田胃散

Pays: Taïwan

Langue: chinois

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

Ingrédients actifs:

SODIUM BICARBONATE ( EQ TO SODIUM HYDROGEN CARBONATE);;ALUMINUM SILICATE;;CALCIUM CARBONATE;;MAGNESIUM CARBONATE;;BIOTAMYLASE;;CINNAMON POWDER (CINNAMON CORTEX POWDER);;FENNEL (FOENICULUM);;MYRISTICA POWDER;;CLOVE POWDER;;PICRASMAE LIGNUM POWDER;;GENTIAN POWDER;;LEMON CONCENTRATE

Disponible depuis:

幼祥實業股份有限公司 台北巿新東街15巷13號1樓 (20854552)

forme pharmaceutique:

散劑

Composition:

MYRISTICA POWDER (2816200601) 20MG; SODIUM BICARBONATE ( EQ TO SODIUM HYDROGEN CARBONATE) (4008000700) 625MG; BIOTAMYLASE (4400003200) 33MG; CALCIUM CARBONATE (5604001200) (PPT) 133MG; MAGNESIUM CARBONATE (5604002400) 26MG; CINNAMON POWDER (CINNAMON CORTEX POWDER) (5610000103) 92MG; FENNEL (FOENICULUM) (5610000300) 24MG; GENTIAN POWDER (5616000802) 15MG; CLOVE POWDER (7200000301) 12MG; PICRASMAE LIGNUM POWDER (9200015402) 15MG; ALUMINUM SILICATE (9600002000) (SYN.) 280MG; LEMON CONCENTRATE (9600033402) 22MG

Unités en paquet:

袋裝;;罐裝

classe:

製 劑

Type d'ordonnance:

須經醫師指示使用

Fabriqué par:

OHTA'S ISAN CO. LTD. 3-2 SENGOKU, 2-CHOME BUNKYO-KU TOKYO JP

indications thérapeutiques:

消化不良、食慾不振、胃酸過多、胃炎

Descriptif du produit:

註銷日期: 1993/03/18; 註銷理由: 賦形劑變更; 有效日期: 1991/12/17; 英文品名: OHTA'S ISAN

Statut de autorisation:

已註銷

Date de l'autorisation:

1980-12-17

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