Orange Book product · Generic (ANDA)
CALCITRIOL
CALCITRIOL
At a glance
Feb 03, 2020
Approved
Generic (ANDA)
Application
AP
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Feb 03, 2020
6 yr 6 mo ago
Today
Pharmaceutical detail
Active ingredient
CALCITRIOL
Strength
0.001MG/ML
Dosage form
INJECTABLE
Route
INJECTION
TE code
AP
Application
ANDA 211030
Product number
001
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of CALCITRIOL
- 2009VECTICALBrand (NDA)
NDA 022087 · GALDERMA LABS LP
- 1998ROCALTROLBrand (NDA)
NDA 021068 · ESJAY PHARMA
- 1986CALCIJEXBrand (NDA)
NDA 018874 · ABBVIE
- —ROCALTROLBrand (NDA)
NDA 018044 · ESJAY PHARMA
- 2026CALCITRIOLGeneric (ANDA)
ANDA 219796 · HUMANWELL PURACAP
- 2023CALCITRIOLGeneric (ANDA)
ANDA 203973 · ANDA REPOSITORY
- 2019CALCITRIOLGeneric (ANDA)
ANDA 204556 · SUN PHARM
- 2018CALCITRIOLGeneric (ANDA)
ANDA 209798 · RISING
- 2017CALCITRIOLGeneric (ANDA)
ANDA 203289 · AMNEAL PHARMS
- 2014CALCITRIOLGeneric (ANDA)
ANDA 091356 · ONESOURCE SPECIALTY
- 2013CALCITRIOLGeneric (ANDA)
ANDA 091174 · BIONPHARMA
- 2008CALCITRIOLGeneric (ANDA)
ANDA 078066 · LONG GROVE PHARMS
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.
