安新Ｂ１２口服液

Valsts: Taivāna

Valoda: ķīniešu

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

Aktīvā sastāvdaļa:

PYRIDOXINE HCL;;CYANOCOBALAMIN (VIT B12);;ASPARTATE MAGNESIUM L-;;ASPARTATE POTASSIUM L- (eq to POTASSIUM L-ASPARTATE);;NIACINAMIDE (NICOTINAMIDE);;GLUCURONIC ACID;;ASCORBIC ACID (VIT C);;SODIUM PANTOTHENATE;;RIBOFLAVIN (VIT B2);;TAURINE (EQ TO 2-AMINOETHANE SULFONIC ACID);;THIAMINE HYDROCHLORIDE

Pieejams no:

安主藥化工業股份有限公司 彰化巿中華西路３２２號 (59152967)

Zāļu forma:

液劑

Kompozīcija:

ASPARTATE MAGNESIUM L- (4020100432) 100MG; ASPARTATE POTASSIUM L- (eq to POTASSIUM L-ASPARTATE) (4020100442) 100MG; GLUCURONIC ACID (5656400100) 100MG; NIACINAMIDE (NICOTINAMIDE) (8810000300) 10MG; THIAMINE HYDROCHLORIDE (8810100900) 10MG; RIBOFLAVIN (VIT B2) (8810200400) 2MG; PYRIDOXINE HCL (8810600300) 5MG; CYANOCOBALAMIN (VIT B12) (8811200300) 5MCG; SODIUM PANTOTHENATE (8812300300) 10MG; ASCORBIC ACID (VIT C) (8816000100) 100MG; TAURINE (EQ TO 2-AMINOETHANE SULFONIC ACID) (9200000900) 100MG

Vienības iepakojumā:

瓶裝

Klase:

製　劑

Receptes veids:

須經醫師指示使用

Ražojis:

安主藥化工業股份有限公司 彰化巿中華西路３２２號 TW

Ārstēšanas norādes:

消除疲勞、營養障礙、維護肝臟正常功能、皮膚炎、口唇炎、口角炎、舌炎、貧血

Produktu pārskats:

註銷日期: 1988/12/31; 註銷理由: 安用科更新資料; 有效日期: 1986/09/22; 英文品名: ANSIE B12 ORAL LIQUID

Autorizācija statuss:

已註銷

Autorizācija datums:

1970-09-22