Quick answers
- What is Allegra Allergy?
- Allegra Allergy is a brand name of Fexofenadine and Fexofenadine and pseudoephedrine, an over-the-counter medicine. The FDA NDC Directory lists 17 Allegra Allergy products in 7 strengths and forms.
- Who makes Allegra Allergy?
- Chattem Sanofi holds the FDA application for Allegra Allergy (NDA020786, approved December 24, 1997). 4 other companies (repackagers or distributors) also list Allegra Allergy products.
- Is there a generic or store brand of Allegra Allergy?
- Yes. The FDA NDC Directory lists 90 other products with the same active ingredients, strength and form as a Allegra Allergy product, 89 of them generic or store brands. Ask your pharmacist whether one is right for you.
- Has Allegra Allergy been recalled?
- No recall linked to Allegra Allergy products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Allegra Allergy is
Each Allegra Allergy product as listed in the FDA NDC Directory, by active ingredient, strength and form, with its official label. “Same medicine, other names” counts the other products with exactly the same active ingredients, strength and form (generic versions, store brands and other brands); inactive ingredients can differ.
Fexofenadine · over-the-counter medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| fexofenadine hydrochloride 180 mg tablet, coated (oral) | Allegra Allergy | 8 products, 7 companies | DailyMed |
| fexofenadine hydrochloride 180 mg tablet, film coated (oral) | Allegra Allergy, Allegra Allergy 24 hour, Allegra Hives 24hr | 41 products, 34 companies | DailyMed |
| fexofenadine hydrochloride 30 mg tablet, orally disintegrating (oral) | Childrens Allegra Allergy | None listed | DailyMed |
| fexofenadine hydrochloride 30 mg/5 mL suspension (oral) | Childrens Allegra Allergy, Childrens Allegra Hives | 14 products, 11 companies | DailyMed |
| fexofenadine hydrochloride 60 mg tablet, film coated (oral) | Allegra Allergy | 9 products, 9 companies | DailyMed |
Its page quotes the Drug Facts label and lists every brand and store brand: Fexofenadine →
Fexofenadine and pseudoephedrine · over-the-counter medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| fexofenadine hydrochloride 180 mg · pseudoephedrine hydrochloride 240 mg tablet, film coated, extended release (oral) | Allegra-D Allergy and Congestion | 2 products, 2 companies | DailyMed |
| fexofenadine hydrochloride 60 mg · pseudoephedrine hydrochloride 120 mg tablet, film coated, extended release (oral) | Allegra-D Allergy and Congestion, Allegra-D | 16 products, 15 companies | DailyMed |
Its page quotes the Drug Facts label and lists every brand and store brand: Fexofenadine and pseudoephedrine →
FDA approval
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
Companies that list Allegra Allergy
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Allegra Allergy products.
- Chattem, Inc.12 products
- A-S Medication Solutions2 products
- Select Consumer Group1 product
- Lil' Drug Store Products, Inc1 product
- Navajo Manufacturing Company Inc.1 product
Recalls
No recall linked to Allegra Allergy products (by their NDC code or label) appears in the FDA enforcement reports.
Sources
- NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug labeling (SPL, openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
- NADAC (National Average Drug Acquisition Cost) 2026 — Centers for Medicare & Medicaid Services (CMS), data.medicaid.gov, list of November 4, 2026, retrieved November 7, 2026
Which names get a brand page: a name the NDC Directory lists for a medicine, held by one company (the FDA application holder, or the company named on most of its products), that is not just a description, and that is not the only product of its medicine.