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Purple Book reference family · 351(a) biologic

belantamab mafodotin-blmf (Blenrep)

belantamab mafodotin-blmf is an FDA-licensed reference biologic from GlaxoSmithKline LLC.

351(a) biologicBLA 761440 GlaxoSmithKline LLC
Biosimilars
0
Interchangeables
0
Listed patents
0
Reference approved
2025

Reference product

Originator biologic
351(a)BLA 761440

Blenrep belantamab mafodotin-blmf

GlaxoSmithKline LLC

View full reference-product record
Approved
Marketing
Rx
Center
CDER
Patents
None listed

Exclusivity & patent cliffs

Protection horizon
  1. Reference approval

    Approval date of the reference belantamab mafodotin-blmf product.

    11 mo ago

belantamab mafodotin-blmf: frequently asked questions

Reference exclusivity, biosimilars, interchangeability, and patents for this molecule, from the FDA Purple Book.

Built from official FDA Purple Book records (monthly downloads, the Advanced Search interface, and the published Patent List), with reference-product, license-type, and exclusivity context for belantamab mafodotin-blmf.

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Agent CTA Background

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