Quick answers
- What is Robitussin?
- Robitussin is a brand name of Dextromethorphan, Dextromethorphan, guaifenesin and phenylephrine, Acetaminophen and Dextromethorphan and doxylamine, an over-the-counter medicine. The FDA NDC Directory lists 12 Robitussin products in 8 strengths and forms.
- Who makes Robitussin?
- Haleon US Holdings LLC lists 8 of the 12 Robitussin products in the FDA NDC Directory.
- Is there a generic or store brand of Robitussin?
- Yes. The FDA NDC Directory lists 133 other products with the same active ingredients, strength and form as a Robitussin product, 133 of them generic or store brands. Ask your pharmacist whether one is right for you.
- Has Robitussin been recalled?
- No recall linked to Robitussin products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Robitussin is
Each Robitussin 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.
Dextromethorphan · over-the-counter medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| dextromethorphan hydrobromide 15 mg capsule, liquid filled (oral) | Robitussin Direct Cough, Robitussin Long-Acting Coughgels | 20 products, 15 companies | DailyMed |
| dextromethorphan hydrobromide 15 mg tablet, chewable (oral) | ROBITUSSIN LONG-ACTING COUGH Soft CHEWS | None listed | DailyMed |
| dextromethorphan hydrobromide 30 mg/5 mL suspension, extended release (oral) | Robitussin 12 Hour Cough Relief | 14 products, 12 companies | DailyMed |
| dextromethorphan hydrobromide 7.5 mg/5 mL liquid (oral) | Childrens Robitussin Cough Long-Acting | None listed | DailyMed |
Its page quotes the Drug Facts label and lists every brand and store brand: Dextromethorphan →
Dextromethorphan, guaifenesin and phenylephrine · over-the-counter medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| dextromethorphan hydrobromide 10 mg/5 mL · guaifenesin 100 mg/5 mL · phenylephrine hydrochloride 5 mg/5 mL liquid (oral) | Robitussin Peak Cold Multi-Symptom Cold | 9 products, 7 companies | DailyMed |
| dextromethorphan hydrobromide 5 mg/5 mL · guaifenesin 50 mg/5 mL · phenylephrine hydrochloride 2.5 mg/5 mL liquid (oral) | Childrens Robitussin Cough and Cold CF | 2 products, 2 companies | DailyMed |
Its page quotes the Drug Facts label and lists every brand and store brand: Dextromethorphan, guaifenesin and phenylephrine →
Acetaminophen · over-the-counter medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| acetaminophen 500 mg tablet, coated (oral) | Robitussin Direct Sore Throat Pain | 88 products, 49 companies | DailyMed |
Its page quotes the Drug Facts label and lists every brand and store brand: Acetaminophen →
Dextromethorphan and doxylamine · over-the-counter medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| dextromethorphan hydrobromide 15 mg · doxylamine succinate 6.25 mg tablet, chewable (oral) | ROBITUSSIN Nighttime Cough DM Soft CHEWS | None listed | DailyMed |
Its page quotes the Drug Facts label and lists every brand and store brand: Dextromethorphan and doxylamine →
FDA approval
- ANDA: Abbreviated New Drug Application: how a generic version is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| ANDA091135 | Tris Pharma Inc | May 25, 2012 | 4 |
Companies that list Robitussin
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Robitussin products.
- Haleon US Holdings LLC12 products
Recalls
No recall linked to Robitussin 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.