Calcitriol
- Product NDC
- 71335-0901
- 11-digit product format
- 713350901
- Labeler code
- 71335
- Product ID
- 71335-0901_6fb33463-e475-4067-957a-271d89a78d13
- 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
- 2013-05-29
- Marketing end
- 0000-00-00
- Substance
- CALCITRIOL
- Active strength
- 1 ug/1
- Pharmacologic classes
- Cholecalciferol [CS],Vitamin D3 Analog [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-0901-1 | 71335090101 | 30 CAPSULE, LIQUID FILLED in 1 BOTTLE (71335-0901-1) | 2018-07-16 | 0000-00-00 | No | No | Current |
| 71335-0901-2 | 71335090102 | 8 CAPSULE, LIQUID FILLED in 1 BOTTLE (71335-0901-2) | 2018-07-16 | 0000-00-00 | No | No | Current |
| 71335-0901-3 | 71335090103 | 28 CAPSULE, LIQUID FILLED in 1 BOTTLE (71335-0901-3) | 2018-07-16 | 0000-00-00 | No | No | Current |
| 71335-0901-4 | 71335090104 | 90 CAPSULE, LIQUID FILLED in 1 BOTTLE (71335-0901-4) | 2018-07-16 | 0000-00-00 | No | No | Current |