NDC product
Cetirizine Hydrochloride 10 mg
NDC 10267-3579 · Contract Pharmacal Corp.
Key facts
| Product NDC | 10267-3579 |
|---|---|
| Proprietary name | Cetirizine Hydrochloride 10 mg |
| Nonproprietary name | Cetirizine Hydrochloride 10 mg |
| Substances | CETIRIZINE HYDROCHLORIDE |
| Dosage form | TABLET, FILM COATED |
| Route | ORAL |
| Labeler | Contract Pharmacal Corp. |
| Product type | HUMAN OTC DRUG |
| Marketing category | ANDA |
| Application number | ANDA076047 |
| Pharmacologic classes | Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC] |
| Marketing start | Apr 16, 2025 |
| 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: