Register entry
- Registered sites
- 0
- Active NDC listings
- 3
- Live patents
- 15
- Countries
- 0
Catalogue
Drug listings by form and route
33 active NDC listings: 3 human prescription drug. By marketing category: NDA 3.
| Dosage form | NDCs |
|---|---|
| tablet | 3 |
| Route | NDCs |
|---|---|
| oral | 3 |
| Labeller name on the listing | NDCs |
|---|---|
| zevra therapeutics, inc. | 3 |
Exclusivity
Patents and exclusivities
15| Patent | Product | Covers | Expiry |
|---|---|---|---|
| 8748413 | APADAZacetaminophen; benzhydrocodone hydrochloride | substance, product | Jul 2030 |
| 8828978 | APADAZacetaminophen; benzhydrocodone hydrochloride | product | Jul 2030 |
| 9132125 | APADAZacetaminophen; benzhydrocodone hydrochloride | substance, product | Jul 2030 |
| 9549923 | APADAZacetaminophen; benzhydrocodone hydrochloride | substance, product | Jul 2030 |
| 8461137 | APADAZacetaminophen; benzhydrocodone hydrochloride | substance, product | Feb 2031 |
Catalogue
Marketed products
3| Brand | Generic name | Form / route | NDC |
|---|---|---|---|
| APADAZ | Benzhydrocodone and Acetaminophen | tablet, oral | 70040-0145NDA |
| APADAZ | Benzhydrocodone and Acetaminophen | tablet, oral | 70040-0167NDA |
| APADAZ | Benzhydrocodone and Acetaminophen | tablet, oral | 70040-0189NDA |
Enquiry
Common questions
- Is Zevra Therapeutics, Inc. FDA approved?
- Zevra Therapeutics, Inc. holds no registered establishment of its own; 3 drug products are listed under its name in the National Drug Code Directory, made at sites registered to other firms.
- What drugs does Zevra Therapeutics, Inc. make?
- 3 products are listed under Zevra Therapeutics, Inc. in the openFDA NDC Directory, most often as tablet. The full breakdown by dosage form and route is above. A listing count is not a sales figure.
Compiled from FDA establishment registrations, the openFDA NDC Directory, the Orange Book and the FDA drug shortage database. Not claimed by the company. Sources and methodology.