NDC product
Children Allergy
NDC 0363-2600 · Walgreens
Key facts
| Product NDC | 0363-2600 |
|---|---|
| Proprietary name | Children Allergy |
| Nonproprietary name | Fexofenadine HCL |
| Substances | FEXOFENADINE HYDROCHLORIDE |
| Dosage form | SUSPENSION |
| Route | ORAL |
| Labeler | Walgreens |
| Product type | HUMAN OTC DRUG |
| Marketing category | ANDA |
| Application number | ANDA203330 |
| Pharmacologic classes | Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC] |
| Marketing start | Oct 31, 2023 |
| Marketing end | Mar 1, 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