Calcitriol

Product NDC
71335-1782
11-digit product format
713351782
Labeler code
71335
Product ID
71335-1782_f099f944-13e9-42fe-8759-b2018871d968
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Calcitriol
Dosage form
CAPSULE, LIQUID FILLED
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA091174
Marketing category
ANDA
Marketing start
2018-06-12
Substance
CALCITRIOL
Active strength
.5 ug/1
Pharmacologic classes
Cholecalciferol [CS], Vitamin D3 Analog [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data

Finished product
Yes
Brand name base
Calcitriol
Listing expiration
2026-12-31

Related Records

Active Ingredients

IngredientStrength
CALCITRIOL.5 ug/1

Harmonized Identifiers

FieldValues
UniiFXC9231JVH
Rxcui308868

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
FXC9231JVHCALCITRIOL32222-06-3CALCITRIOL

Packages

Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
71335-1782-17133517820130 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (71335-1782-1) 2021-08-270000-00-00NoNoCurrent
71335-1782-2713351782028 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (71335-1782-2) 2021-08-270000-00-00NoNoCurrent
71335-1782-37133517820328 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (71335-1782-3) 2021-08-270000-00-00NoNoCurrent
71335-1782-47133517820490 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (71335-1782-4) 2021-08-270000-00-00NoNoCurrent

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Calcitriol Capsule, Liquid Filled Rx onlyBryant Ranch Prepack2025-03-31HUMAN PRESCRIPTION DRUG LABEL103