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盐酸左西替利嗪口服溶液 - NMPA Drug Approval Details

Approvals/NMPA/Levocetirizine Dihydrochloride Oral Solution

Approved

化学药品

Levocetirizine Dihydrochloride Oral Solution

浙江核力欣健药业有限公司🇨🇳 National Medical Products Administration

Approval Date: Dec 30, 2022
Approval ID: 567ba2f3ed18de55
Company: 浙江核力欣健药业有限公司
Type: 化学药品

Approval Details

Approval Id: 567ba2f3ed18de55
Approval Number: 国药准字H20223974
Generic Name: 盐酸左西替利嗪口服溶液
Generic Name En: Levocetirizine Dihydrochloride Oral Solution
Drug Type: 化学药品
Dosage Form: 口服溶液剂
Strength: 0.05%（150ml:75mg）
Reg Date: 2022-12-30
Company Name: 浙江核力欣健药业有限公司
Company Address: 浙江省湖州市三天门路2号
Production Company Name: 浙江康恩贝制药股份有限公司
Production Company Address: 浙江省兰溪市康恩贝大道1号
Company Detail Path: /organization/b7d743176d4a098a/zhe-jiang-he-li-xin-jian-yao-ye-you-xian-gong-si
Production Company Detail Path: /organization/0fc26cf18a019dde/zhejiang-conba-pharmaceutical-co-ltd

Approved

Quick Info

Agency

NMPA

Country

🇨🇳

Approval Date

Dec 30, 2022

Approval ID

567ba2f3ed18de55

Type

化学药品

Back to NMPA Approvals