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倍力腾 - NMPA Drug Approval Details
Approvals
/
NMPA
/
Belimumab powder for concentrate for solution for infusion
Approved
生物制品
Belimumab powder for concentrate for solution for infusion
GLAXOSMITHKLINE (IRELAND) LIMITED
🇨🇳 National Medical Products Administration
Approval Date
Dec 10, 2019
Approval ID
7ucizL9nB5u
Company
GLAXOSMITHKLINE (IRELAND) LIMITED
Type
生物制品
Approval Details
Approval Id
7ucizL9nB5u
Approval Number
S20190033
Generic Name
注射用贝利尤单抗
Generic Name En
Belimumab powder for concentrate for solution for infusion
Trade Name
倍力腾
Drug Type
生物制品
Dosage Form
注射剂
Strength
400mg/瓶
Reg Date
2019-12-10
Expired Date
2024-07-11
Company Name
GLAXOSMITHKLINE (IRELAND) LIMITED
Company Address
12 Riverwalk, Citywest Business Campus, Dublin 24, Ireland
Production Company Name
glaxosmithkline manufacturing s.p.a.
Production Company Address
Strada Provinciale Asolana no. 90, San Polo di Torrile, Parma 43056, Italy
Company Detail Path
/organization/glaxosmithkline-ireland-limited
Approved
Quick Info
Agency
NMPA
Country
🇨🇳
Approval Date
Dec 10, 2019
Approval ID
7ucizL9nB5u
Type
生物制品
Back to NMPA Approvals