Calcitriol
- Product NDC
- 72162-1031
- 11-digit product format
- 721621031
- Labeler code
- 72162
- Product ID
- 72162-1031_34f54402-2dd2-3eeb-e063-6394a90ab403
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Calcitriol
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA075765
- Marketing category
- ANDA
- Marketing start
- 2025-05-12
- Substance
- CALCITRIOL
- Active strength
- .25 ug/1
- Pharmacologic classes
- Cholecalciferol [CS], Vitamin D3 Analog [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| FXC9231JVH | CALCITRIOL | 32222-06-3 | CALCITRIOL |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-1031-1 | 72162103101 | 100 CAPSULE, LIQUID FILLED in 1 BOTTLE (72162-1031-1) | 2025-05-12 | No | No | Historical |