NDC product
Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride
NDC 0363-0044 · Walgreens Company
Key facts
| Product NDC | 0363-0044 |
|---|---|
| Proprietary name | Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride |
| Nonproprietary name | Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride |
| Substances | FEXOFENADINE HYDROCHLORIDE, PSEUDOEPHEDRINE HYDROCHLORIDE |
| Dosage form | TABLET, EXTENDED RELEASE |
| Route | ORAL |
| Labeler | Walgreens Company |
| Product type | HUMAN OTC DRUG |
| Marketing category | ANDA |
| Application number | ANDA215434 |
| Pharmacologic classes | Adrenergic alpha-Agonists [MoA], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC], alpha-Adrenergic Agonist [EPC] |
| Marketing start | Mar 31, 2022 |
| 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: