Quick answers
- What is Hydrocodone APAP?
- Hydrocodone APAP is a brand name of Hydrocodone bitartrate and acetaminophen, a prescription medicine. The FDA NDC Directory lists 1 Hydrocodone APAP product in 1 strength and form.
- Who makes Hydrocodone APAP?
- Ascent Pharms Inc holds the FDA application for Hydrocodone APAP (ANDA211487, approved November 7, 2018).
- Is there a generic or store brand of Hydrocodone APAP?
- Yes. The FDA NDC Directory lists 45 other products with the same active ingredients, strength and form as a Hydrocodone APAP product, 45 of them generic. Ask your pharmacist whether one is right for you.
- Has Hydrocodone APAP been recalled?
- No recall linked to Hydrocodone APAP products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Hydrocodone APAP is
Each Hydrocodone APAP 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.
Hydrocodone bitartrate and acetaminophen · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| acetaminophen 325 mg · hydrocodone bitartrate 7.5 mg tablet (oral) | Hydrocodone APAP | 45 products, 24 companies | DailyMed |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Hydrocodone bitartrate and acetaminophen →
FDA approval
- ANDA: Abbreviated New Drug Application: how a generic version is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| ANDA211487 | Ascent Pharms Inc | November 7, 2018 | 1 |
Companies that list Hydrocodone APAP
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Hydrocodone APAP products.
- Direct_Rx1 product
Recalls
No recall linked to Hydrocodone APAP 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.