Orange Book product · Generic (ANDA)
HALCINONIDE
HALCINONIDE
At a glance
May 29, 2024
Approved
Generic (ANDA)
Application
AT
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
May 29, 2024
2 yr 1 mo ago
Today
Pharmaceutical detail
Active ingredient
HALCINONIDE
Strength
0.1%
Dosage form
SOLUTION
Route
TOPICAL
TE code
AT
Application
ANDA 217671
Product number
001
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
Yes
Active-ingredient family
View full familyGeneric (ANDA) of HALCINONIDE
- —HALOGBrand (NDA)
NDA 017556 · SUN PHARM INDS INC
- —HALOGBrand (NDA)
NDA 017818 · WESTWOOD SQUIBB
- —HALOG-EBrand (NDA)
NDA 018234 · SUN PHARM INDS INC
- —HALOGBrand (NDA)
NDA 018125 · BRISTOL MYERS SQUIBB
- —HALOGBrand (NDA)
NDA 017824 · SUN PHARM INDS INC
- —HALOGBrand (NDA)
NDA 017823 · SUN PHARM INDS INC
- 2021HALCINONIDEGeneric (ANDA)
ANDA 214723 · CHARTWELL RX
- 2019HALCINONIDEGeneric (ANDA)
ANDA 211027 · MYLAN
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.
