NDC product
Loratadine and Pseudoephedrine
NDC 0363-0725 · Walgreen Company
Key facts
| Product NDC | 0363-0725 |
|---|---|
| Proprietary name | Loratadine and Pseudoephedrine |
| Nonproprietary name | Loratadine and Pseudoephedrine |
| Substances | LORATADINE, PSEUDOEPHEDRINE SULFATE |
| Dosage form | TABLET, FILM COATED, EXTENDED RELEASE |
| Route | ORAL |
| Labeler | Walgreen Company |
| Product type | HUMAN OTC DRUG |
| Marketing category | ANDA |
| Application number | ANDA076557 |
| Pharmacologic classes | Adrenergic alpha-Agonists [MoA], alpha-Adrenergic Agonist [EPC] |
| Marketing start | Nov 7, 2013 |
| 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: