Quick answers
- What is Zantac 360?
- Zantac 360 is a brand name of Famotidine, an over-the-counter medicine. The FDA NDC Directory lists 6 Zantac 360 products in 1 strength and form.
- Who makes Zantac 360?
- Aurobindo Pharma holds the FDA application for Zantac 360 (ANDA206531, approved April 26, 2016). 4 other companies (repackagers or distributors) also list Zantac 360 products.
- Is there a generic or store brand of Zantac 360?
- Yes. The FDA NDC Directory lists 71 other products with the same active ingredients, strength and form as a Zantac 360 product, 68 of them generic or store brands. Ask your pharmacist whether one is right for you.
- Has Zantac 360 been recalled?
- No recall linked to Zantac 360 products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Zantac 360 is
Each Zantac 360 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.
Famotidine · over-the-counter medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| famotidine 20 mg tablet, film coated (oral) | Zantac 360, Zantac 360 2 per blister 6 blisters, Zantac 360 Cool Mint | 71 products, 48 companies | DailyMed |
Its page quotes the Drug Facts label and lists every brand and store brand: Famotidine →
FDA approval
- ANDA: Abbreviated New Drug Application: how a generic version is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| ANDA206531 | Aurobindo Pharma | April 26, 2016 | 6 |
Companies that list Zantac 360
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Zantac 360 products.
- Chattem, Inc.2 products
- JC World Bell Wholesale Co., Inc.1 product
- Select Consumer Group LLC1 product
- Navajo Manufacturing Company Inc.1 product
- Lil' Drug Store Products, Inc1 product
Recalls
No recall linked to Zantac 360 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.