Orange Book product · Generic (ANDA)
HALCINONIDE
HALCINONIDE
At a glance
Aug 12, 2019
Approved
Generic (ANDA)
Application
AB
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Aug 12, 2019
6 yr 11 mo ago
Today
Pharmaceutical detail
Active ingredient
HALCINONIDE
Strength
0.1%
Dosage form
CREAM
Route
TOPICAL
TE code
AB
Application
ANDA 211027
Product number
001
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
No
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
- 2024HALCINONIDEGeneric (ANDA)
ANDA 217671 · ENCUBE
- 2021HALCINONIDEGeneric (ANDA)
ANDA 214723 · CHARTWELL RX
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.
