Orange Book product · Generic (ANDA)
GLYBURIDE
GLYBURIDE
At a glance
Sep 30, 2015
Approved
Generic (ANDA)
Application
AB2
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Sep 30, 2015
10 yr 11 mo ago
Today
Pharmaceutical detail
Active ingredient
GLYBURIDE
Strength
1.25MG
Dosage form
TABLET
Route
ORAL
TE code
AB2
Application
ANDA 206079
Product number
001
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of GLYBURIDE
- 1992GLYBURIDE (MICRONIZED)Brand (NDA)
NDA 020055 · SANOFI AVENTIS US
- 1992GLYNASEBrand (NDA)
NDA 020051 · PFIZER
- 1984DIABETABrand (NDA)
NDA 017532 · SANOFI AVENTIS US
- 1984MICRONASEBrand (NDA)
NDA 017498 · PFIZER
- 2019GLYBURIDEGeneric (ANDA)
ANDA 206483 · ORIENT PHARMA CO LTD
- 2019GLYBURIDEGeneric (ANDA)
ANDA 203379 · CADILA PHARMS LTD
- 2016GLYBURIDEGeneric (ANDA)
ANDA 206749 · ZYDUS PHARMS
- 2016GLYBURIDEGeneric (ANDA)
ANDA 203581 · CHARTWELL RX
- 2011GLYBURIDEGeneric (ANDA)
ANDA 090937 · HERITAGE
- 2007GLYBURIDEGeneric (ANDA)
ANDA 077537 · AUROBINDO PHARMA
- 2003GLYBURIDE (MICRONIZED)Generic (ANDA)
ANDA 075890 · HIKMA
- 2002GLYBURIDEGeneric (ANDA)
ANDA 075947 · ACTAVIS ELIZABETH
Listed patents
No patents are listed against this product in the Orange Book. Listed patents reflect those the NDA holder submits under 21 U.S.C. 355 and are not exhaustive.
