Calcitriol
- Product NDC
- 71335-2095
- 11-digit product format
- 713352095
- Labeler code
- 71335
- Product ID
- 71335-2095_6d067128-2c84-4a19-a58b-98c7ea6eae10
- 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
- 2016-08-25
- Marketing end
- 0000-00-00
- Substance
- CALCITRIOL
- Active strength
- 0 ug/1
- Pharmacologic classes
- Cholecalciferol [CS], Vitamin D3 Analog [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
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 | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-2095-1 | 71335209501 | 30 CAPSULE, LIQUID FILLED in 1 BOTTLE (71335-2095-1) | 2022-05-23 | 0000-00-00 | No | No | Current |
| 71335-2095-2 | 71335209502 | 28 CAPSULE, LIQUID FILLED in 1 BOTTLE (71335-2095-2) | 2022-05-23 | 0000-00-00 | No | No | Current |
| 71335-2095-3 | 71335209503 | 90 CAPSULE, LIQUID FILLED in 1 BOTTLE (71335-2095-3) | 2022-05-23 | 0000-00-00 | No | No | Current |