Quick answers
- What is Astepro Allergy?
- Astepro Allergy is a brand name of Azelastine, an over-the-counter medicine. The FDA NDC Directory lists 2 Astepro Allergy products in 1 strength and form.
- Who makes Astepro Allergy?
- Bayer Hlthcare holds the FDA application for Astepro Allergy (NDA213872, approved June 17, 2021).
- Is there a generic or store brand of Astepro Allergy?
- Yes. The FDA NDC Directory lists 7 other products with the same active ingredients, strength and form as a Astepro Allergy product, 7 of them generic or store brands. Ask your pharmacist whether one is right for you.
- Has Astepro Allergy been recalled?
- No recall linked to Astepro Allergy products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Astepro Allergy is
Each Astepro 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.
Azelastine · over-the-counter medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| azelastine hydrochloride 205.5 ug spray, metered (nasal) | Astepro Allergy, Children Astepro Allergy | 7 products, 6 companies | DailyMed |
Its page quotes the Drug Facts label and lists every brand and store brand: Azelastine →
FDA approval
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| NDA213872 | Bayer Hlthcare | June 17, 2021 | 2 |
Companies that list Astepro Allergy
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Astepro Allergy products.
- Bayer HealthCare LLC.2 products
Recalls
No recall linked to Astepro 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.