Orange Book product · Generic (ANDA)
SOTRET
ISOTRETINOIN
At a glance
Dec 24, 2002
Approved
Generic (ANDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Dec 24, 2002
23 yr 10 mo ago
Today
Pharmaceutical detail
Active ingredient
ISOTRETINOIN
Strength
10MG
Dosage form
CAPSULE
Route
ORAL
TE code
Not listed
Application
ANDA 076041
Product number
001
Marketing status
DISCN
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of ISOTRETINOIN
- 2019ABSORICA LDBrand (NDA)
NDA 211913 · SUN PHARM
- 2012ABSORICABrand (NDA)
NDA 021951 · SUN PHARM INDS INC
- 1982ACCUTANEBrand (NDA)
NDA 018662 · HOFFMANN LA ROCHE
- 2025ISOTRETINOINGeneric (ANDA)
ANDA 216097 · AMNEAL PHARMS NY
- 2025ISOTRETINOINGeneric (ANDA)
ANDA 216633 · ZYDUS PHARMS
- 2024ISOTRETINOINGeneric (ANDA)
ANDA 218194 · AUROBINDO PHARMA
- 2023ISOTRETINOINGeneric (ANDA)
ANDA 211568 · ZYDUS PHARMS
- 2021ISOTRETINOINGeneric (ANDA)
ANDA 212333 · UPSHER SMITH LABS
- 2021ISOTRETINOINGeneric (ANDA)
ANDA 213571 · UPSHER SMITH LABS
- 2021ISOTRETINOINGeneric (ANDA)
ANDA 205063 · ACTAVIS LABS FL
- 2017ISOTRETINOINGeneric (ANDA)
ANDA 207792 · AMNEAL PHARMS NY
- 2013ZENATANEGeneric (ANDA)
ANDA 202099 · DR REDDYS LABS LTD
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.
