NDC product
Fexofenadine Hydrochloride
NDC 71309-091 · Safrel Pharmaceuticals, LLC.
Key facts
| Product NDC | 71309-091 |
|---|---|
| Proprietary name | Fexofenadine Hydrochloride |
| Nonproprietary name | Fexofenadine Hydrochloride |
| Substances | FEXOFENADINE HYDROCHLORIDE |
| Dosage form | TABLET |
| Route | ORAL |
| Labeler | Safrel Pharmaceuticals, LLC. |
| Product type | HUMAN OTC DRUG |
| Marketing category | ANDA |
| Application number | ANDA211075 |
| Pharmacologic classes | Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC] |
| Marketing start | Jan 3, 2021 |
| 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: