Calcitriol
- Product NDC
- 71335-0443
- 11-digit product format
- 713350443
- Labeler code
- 71335
- Product ID
- 71335-0443_c5297bbb-79eb-447a-a2e1-25b9966e1bd6
- 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
- 0 ug/1
- Pharmacologic classes
- Cholecalciferol [CS],Vitamin D3 Analog [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record