Calcitriol
- Product NDC
- 50090-6711
- 11-digit product format
- 500906711
- Labeler code
- 50090
- Product ID
- 50090-6711_c8e9e4a3-65ea-411c-b712-51f6c0e8f555
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Calcitriol
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA091174
- Marketing category
- ANDA
- Marketing start
- 2018-06-12
- 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 |
|---|
| 50090-6711-0 | 50090671100 | 30 CAPSULE, LIQUID FILLED in 1 BOTTLE (50090-6711-0) | 2023-09-28 | No | No | Historical |