PARICALCITOL
- Product NDC
- 40051-614
- 11-digit product format
- 400510614
- Labeler code
- 40051
- Product ID
- 40051-614_9604e644-2965-739d-e053-2995a90af129
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- paricalcitol
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Lotus Pharmaceutical Co., Ltd. Nantou Plant
- Application
- ANDA206710
- Marketing category
- ANDA
- Marketing start
- 2017-03-31
- Marketing end
- 0000-00-00
- Substance
- PARICALCITOL
- Active strength
- 4 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 40051-614-11 | 40051061411 | 30 CAPSULE in 1 BOTTLE, PLASTIC (40051-614-11) | 30 capsule | 2017-03-31 | 0000-00-00 | No | No | Current |