Orange Book product · Brand (NDA)
PANRETIN
ALITRETINOIN
Brand (NDA)NDA 020886RX ADVANZ PHARMA
At a glance
Feb 02, 1999
Approved
Brand (NDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Feb 02, 1999
27 yr 9 mo ago
Today
Pharmaceutical detail
Active ingredient
ALITRETINOIN
Strength
EQ 0.1% BASE
Dosage form
GEL
Route
TOPICAL
TE code
Not listed
Application
NDA 020886
Product number
001
Marketing status
RX
Reference listed drug (RLD)
Yes
Reference standard (RS)
Yes
Active-ingredient family
View full familyThis is a reference-listed drug (RLD) — the basis for generic (ANDA) applications. Other products sharing this ingredient are listed below.
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.
