United States · FDA National Drug Code directory
Calcitriol
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 62756-968_fb99b865-fb41-4c92-8db9-7953feed2394
- Product NDC
- 62756-968
- Form
- CAPSULE, LIQUID FILLED
- Composition / generic term
- Calcitriol
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200501
- Source listing expiry
- 20261231
Source-listed ingredients
- CALCITRIOL — .5 ug/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1000 CAPSULE, LIQUID FILLED in 1 BOTTLE (62756-968-18) · 62756-968-18
- 30 CAPSULE, LIQUID FILLED in 1 BOTTLE (62756-968-83) · 62756-968-83
- 100 CAPSULE, LIQUID FILLED in 1 BOTTLE (62756-968-88) · 62756-968-88
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →