Orange Book product · Generic (ANDA)
CALCITRIOL
CALCITRIOL
At a glance
Mar 27, 2006
Approved
Generic (ANDA)
Application
AB
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Mar 27, 2006
20 yr 6 mo ago
Today
Pharmaceutical detail
Active ingredient
CALCITRIOL
Strength
0.25MCG
Dosage form
CAPSULE
Route
ORAL
TE code
AB
Application
ANDA 076917
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
- 2020CALCITRIOLGeneric (ANDA)
ANDA 211030 · GLAND
- 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
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.
