Lantus Purple Book BLA 021081

BLA number
021081
Proprietary names
Lantus
Proper names
insulin glargine
Applicant
Sanofi-Aventis U.S. LLC
Center
CDER
First observed release
2020-05-01
Latest observed release
2026-06-01
Newest archive release
2026-06-01
FDA patent list
No patents listed in the captured FDA patent list; source updated 2025-06-11
Coverage
Present in newest release

Latest Known Product Presentations#

Product, Proprietary name, Proper name table
ProductProprietary nameProper nameLicense typeStrengthDosage formRoutePresentationMarketingLicensureApprovalPatent list provided
001Lantusinsulin glargine351(a)1,000UNITS/10ML (100UNITS/ML)InjectionSubcutaneousMulti-Dose VialRxLicensed2000-04-20
002Lantusinsulin glargine351(a)300UNITS/3ML (100UNITS/ML)InjectionSubcutaneousAutoinjectorRxLicensed2007-04-25
003Lantusinsulin glargine351(a)500UNITS/5ML (100UNITS/ML)InjectionSubcutaneousMulti-Dose VialDiscLicensed2000-04-20
004Lantusinsulin glargine351(a)300UNITS/3ML (100UNITS/ML)InjectionSubcutaneousMulti-Dose CartridgeDiscLicensed2000-04-20

Biosimilar And Interchangeable Products#

BLA, Proprietary name, Proper name table
BLAProprietary nameProper nameLicense typeStatusLatest source
761201Semgleeinsulin glargine-yfgn351(k) InterchangeableRx2026-06-01
761215Rezvoglarinsulin glargine-aglr351(k) InterchangeableRx2026-06-01
761412Langlarainsulin glargine-aldy351(k) InterchangeableRx2026-06-01

Published Patent List#

No patents for this BLA were listed in the FDA Purple Book patent list captured from the source updated 2025-06-11.

Official Monthly Change Events#

Release, Event, Product table
ReleaseEventProductNameLicense typeStatusApplicant
2021-05-01U001Lantus351(a)RxSanofi-Aventis U.S. LLC
2021-05-01U002Lantus351(a)RxSanofi-Aventis U.S. LLC
2021-05-01U003Lantus351(a)DiscSanofi-Aventis U.S. LLC
2021-05-01U004Lantus351(a)DiscSanofi-Aventis U.S. LLC
2020-05-01R001Lantus351(a)RxSanofi-Aventis US LLC
2020-05-01R002Lantus351(a)RxSanofi-Aventis US LLC
2020-05-01R003Lantus351(a)DiscSanofi-Aventis US LLC
2020-05-01R004Lantus351(a)DiscSanofi-Aventis US LLC

Observed Product State History#

Release, Product, Name table
ReleaseProductNameLicense typeMarketingLicensureApproval
2020-05-01001Lantus351(a)RxLicensed2000-04-20
2020-05-01002Lantus351(a)RxLicensed2007-04-25
2020-05-01003Lantus351(a)DiscLicensed2000-04-20
2020-05-01004Lantus351(a)DiscLicensed2000-04-20