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盐酸去氧肾上腺素注射液 - NMPA Drug Approval Details

Approvals/NMPA/Phenylephrine Hydrochloride Injection

Approved

化学药品

Phenylephrine Hydrochloride Injection

海南倍特药业有限公司🇨🇳 National Medical Products Administration

Approval Date: Dec 25, 2024
Approval ID: 8gJy2U4pKT5
Company: 海南倍特药业有限公司
Type: 化学药品

Approval Details

Approval Id: 8gJy2U4pKT5
Approval Number: 国药准字H20249841
Generic Name: 盐酸去氧肾上腺素注射液
Generic Name En: Phenylephrine Hydrochloride Injection
Drug Type: 化学药品
Dosage Form: 注射剂
Strength: 5ml∶0.5mg
Reg Date: 2024-12-25
Company Name: 海南倍特药业有限公司
Company Address: 海口市海口国家高新技术产业开发区药谷一路4号
Production Company Name: 海南倍特药业有限公司
Production Company Address: 海口市海口国家高新技术产业开发区药谷一路4号
Company Detail Path: /organization/80b7c3665f4af734/hai-nan-bei-te-yao-ye-you-xian-gong-si
Production Company Detail Path: /organization/80b7c3665f4af734/hai-nan-bei-te-yao-ye-you-xian-gong-si

Approved

Quick Info

Agency

NMPA

Country

🇨🇳

Approval Date

Dec 25, 2024

Approval ID

8gJy2U4pKT5

Type

化学药品

Back to NMPA Approvals