胃腸藥

Country: Թայվան

language: չինարեն

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

active_ingredient:

SODIUM BICARBONATE ( EQ TO SODIUM HYDROGEN CARBONATE);;MAGNESIUM CARBONATE;;DIASTASE;;NORUMOZANHILUS;;FENNEL POWDER (FOENICULI POWDER);;CASSIA POWDER;;ARALIAE CORTEX POWDER;;MYRISTICA POWDER;;CLOVE POWDER;;ORANGE PEEL;;SWERTIA POWDER;;L-MENTHOL

MAH:

南輝企業股份有限公司 台北巿重慶北路3段113巷55號一樓 (15273204)

pharmaceutical_form:

散劑

composition:

MYRISTICA POWDER (2816200601) 21MG; SODIUM BICARBONATE ( EQ TO SODIUM HYDROGEN CARBONATE) (4008000700) 373MG; MAGNESIUM CARBONATE (5604002400) 51MG; CASSIA POWDER (5610000123) 34MG; FENNEL POWDER (FOENICULI POWDER) (5610000301) 34MG; DIASTASE (5616000700) 51MG; CLOVE POWDER (7200000301) 12MG; L-MENTHOL (8408000302) 1MG; SWERTIA POWDER (9200014901) 7MG; ARALIAE CORTEX POWDER (9200016311) 34MG; NORUMOZANHILUS (9200023900) 370MG; ORANGE PEEL (9600020350) (POWDER)12MG

units_in_package:

罐裝

class:

製 劑

prescription_type:

須由醫師處方使用

manufactured_by:

DOJIN YAKUGYO CO. LTD. 44-18 KOBASHICHO, TENOZEKU, OSAKA. JP

therapeutic_indication:

胃酸過多、消化不良、腹部膨滿

leaflet_short:

註銷日期: 1987/04/08; 註銷理由: 有效期間已屆未能補件; 有效日期: 1985/06/15; 英文品名: ICHOYAKU "DOJIN"

authorization_status:

已註銷

authorization_date:

1976-10-08

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