依諾比隆錠

Pajjiż: 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:

SODIUM BICARBONATE ( EQ TO SODIUM HYDROGEN CARBONATE);;THIAMINE DISULFIDE;;ALRANT PERIC;;CINNAMON POWDER (CINNAMON CORTEX POWDER);;POLYPASE;;DIASTASE;;NOISIRIN (SIMALDRATE);;BIOTAMYLASE;;ZINGER (ZINGIBER);;CALCIUM CARBONATE;;VITAMIN U (METHYLMETHIONINE SULFONIUM CHLORIDE);;SCOPOLIA EXTRACT

Disponibbli minn:

大中有限公司 台北巿瑞安街２５４號４樓 (03009407)

Għamla farmaċewtika:

錠劑

Kompożizzjoni:

SCOPOLIA EXTRACT (1208004502) 5MG; SODIUM BICARBONATE ( EQ TO SODIUM HYDROGEN CARBONATE) (4008000700) 66.666MG; BIOTAMYLASE (4400003200) 33.333MG; CALCIUM CARBONATE (5604001200) (PPT) 61.666MG; CINNAMON POWDER (CINNAMON CORTEX POWDER) (5610000103) 16.666MG; DIASTASE (5616000700) 33.333MG; POLYPASE (5616002100) 33.333MG; NOISIRIN (SIMALDRATE) (5616004300) 100MG; THIAMINE DISULFIDE (8810100800) 1MG; VITAMIN U (METHYLMETHIONINE SULFONIUM CHLORIDE) (8827000100) 13.333MG; ALRANT PERIC (9200014600) 16.666MG; ZINGER (ZINGIBER) (9200015000) 16.666MG

Unitajiet fil-pakkett:

瓶裝

Klassi:

製　劑

Tip ta 'preskrizzjoni:

須經醫師指示使用

Manifatturat minn:

HOKUHO YAKUHIN CO. LTD. 6-5-2 HANNANTYO ABENO-KU OSAKA JP

Indikazzjonijiet terapewtiċi:

消化不良、胃酸過多、胃潰瘍、十二指腸潰瘍的疼痛、腸內異狀醱酵胃痛、腹痛

Sommarju tal-prodott:

註銷日期: 1990/02/28; 註銷理由: 移轉（申請商）; 有效日期: 1991/11/06; 英文品名: NOIPILON-ACE TABLETS

L-istatus ta 'awtorizzazzjoni:

已註銷

Data ta 'l-awtorizzazzjoni:

1984-01-30