Orange Book product · Brand (NDA)
THALOMID
THALIDOMIDE
Brand (NDA)NDA 020785TE ABRX BRISTOL-MYERS
At a glance
Jan 17, 2003
Approved
Brand (NDA)
Application
AB
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Jan 17, 2003
23 yr 9 mo ago
Today
Pharmaceutical detail
Active ingredient
THALIDOMIDE
Strength
100MG
Dosage form
CAPSULE
Route
ORAL
TE code
AB
Application
NDA 020785
Product number
002
Marketing status
RX
Reference listed drug (RLD)
Yes
Reference standard (RS)
No
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.
