NDC product
Allergy Relief
NDC 63868-665 · CHAIN DRUG MARKETING ASSOCIATION INC.
Key facts
| Product NDC | 63868-665 |
|---|---|
| Proprietary name | Allergy Relief |
| Nonproprietary name | Cetirizine hydrochloride |
| Substances | CETIRIZINE HYDROCHLORIDE |
| Dosage form | TABLET, COATED |
| Route | ORAL |
| Labeler | CHAIN DRUG MARKETING ASSOCIATION INC. |
| Product type | HUMAN OTC DRUG |
| Marketing category | ANDA |
| Application number | ANDA209274 |
| Pharmacologic classes | Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC] |
| Marketing start | Sep 1, 2018 |
| Marketing end | Jan 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