NDC product
Norepinephrine
NDC 43742-1489 · Deseret Biologicals, Inc.
Key facts
| Product NDC | 43742-1489 |
|---|---|
| Proprietary name | Norepinephrine |
| Nonproprietary name | Norepinephrine (Bitartrate) |
| Substances | NOREPINEPHRINE BITARTRATE |
| Dosage form | LIQUID |
| Route | ORAL |
| Labeler | Deseret Biologicals, Inc. |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Catecholamine [EPC], Catecholamines [CS] |
| Marketing start | May 28, 2019 |
| Listing certified through | Dec 31, 2026 |
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 · Source date: