NDC product
Zemplar
NDC 0074-9036 · AbbVie Inc.
Key facts
| Product NDC | 0074-9036 |
|---|---|
| Proprietary name | Zemplar |
| Nonproprietary name | Paricalcitol |
| Substances | PARICALCITOL |
| Dosage form | CAPSULE, LIQUID FILLED |
| Route | ORAL |
| Labeler | AbbVie Inc. |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Application number | NDA021606 |
| Pharmacologic classes | Ergocalciferols [CS], Vitamin D Analog [EPC], Vitamin D2 Analog [EPC] |
| Marketing start | Apr 20, 2018 |
| Marketing end | Mar 31, 2027 |
At a glance
- 1–9 Package NDCs
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About National Drug Codes (NDC)
The National Drug Code (NDC) is the FDA's product identifier for drugs; the product NDC identifies the labeler and product, and each package adds a package code.
Source: U.S. Food and Drug Administration (FDA), National Drug Code Directory