NDC product
oxymetazoline hydrochloride
NDC 68071-3422 · NuCare Pharmaceuticals,Inc.
Key facts
| Product NDC | 68071-3422 |
|---|---|
| Proprietary name | oxymetazoline hydrochloride |
| Nonproprietary name | oxymetazoline hydrochloride |
| Substances | OXYMETAZOLINE HYDROCHLORIDE |
| Dosage form | SPRAY |
| Route | NASAL |
| Labeler | NuCare Pharmaceuticals,Inc. |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M012 |
| Pharmacologic classes | Imidazolines [CS], Increased Sympathetic Activity [PE], Vasoconstriction [PE], Vasoconstrictor [EPC] |
| Marketing start | Dec 5, 2005 |
| Marketing end | Feb 28, 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