力源口服液

Land: Taiwan

Taal: Chinees

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

Werkstoffen:

ASPARTATE MAGNESIUM;;ASPARTATE POTASSIUM;;THIOCTIC ACID (VIT B14ALPHA-LIPOIC ACID);;GLUCURONIC ACID;;TAURINE (EQ TO 2-AMINOETHANE SULFONIC ACID);;THIAMINE (VITAMIN B1);;RIBOFLAVIN PHOSPHATE;;PYRIDOXINE(VITAMIN B6);;CYANOCOBALAMIN (VIT B12);;ASCORBIC ACID (VIT C);;NIACINAMIDE (NICOTINAMIDE);;SODIUM PANTOTHENATE

Beschikbaar vanaf:

漁人製藥股份有限公司 高雄巿左營區民族一路７０７號 (83648834)

farmaceutische vorm:

內服液劑

Samenstelling:

ASPARTATE MAGNESIUM (4020100430) 400MG; ASPARTATE POTASSIUM (4020100440) 400MG; GLUCURONIC ACID (5656400100) 200MG; THIOCTIC ACID (VIT B14ALPHA-LIPOIC ACID) (5656900700) 5MG; NIACINAMIDE (NICOTINAMIDE) (8810000300) 10MG; THIAMINE (VITAMIN B1) (8810100500) 10MG; RIBOFLAVIN PHOSPHATE (8810200600) 5MG; PYRIDOXINE(VITAMIN B6) (8810600100) 3MG; CYANOCOBALAMIN (VIT B12) (8811200300) 5MCG; SODIUM PANTOTHENATE (8812300300) 10MG; ASCORBIC ACID (VIT C) (8816000100) 150MG; TAURINE (EQ TO 2-AMINOETHANE SULFONIC ACID) (9200000900) 500MG

Eenheden in pakket:

瓶裝

klasse:

製　劑

Prescription-type:

須經醫師指示使用

Geproduceerd door:

漁人製藥股份有限公司 高雄巿左營區民族一路７０７號 TW

therapeutische indicaties:

消除疲勞、增強抵抗力、維護肝臟機能、宿醉、病後衰弱

Product samenvatting:

註銷日期: 1995/04/27; 註銷理由: 中文品名變更;;英文品名變更; 有效日期: 1998/05/25; 英文品名: LE GEN ORAL SOLUTION

Autorisatie-status:

已註銷

Autorisatie datum:

1992-05-23