Register entry
- Registered sites
- 0
- Active NDC listings
- 3
- Live patents
- 0
- Countries
- 0
Catalogue
Drug listings by form and route
33 active NDC listings: 3 human prescription drug. By marketing category: ANDA 2, NDA 1.
| Dosage form | NDCs |
|---|---|
| powder, for solution | 1 |
| solution/ drops | 1 |
| syrup | 1 |
| Route | NDCs |
|---|---|
| oral | 2 |
| ophthalmic | 1 |
| Labeller name on the listing | NDCs |
|---|---|
| akorn | 3 |
Catalogue
Marketed products
3| Brand | Generic name | Form / route | NDC |
|---|---|---|---|
| Dorzolamide Hydrochloride and Timolol Maleate | Dorzolamide Hydrochloride and Timolol Maleate | solution/ drops, ophthalmic | 50383-261NDA |
| Famotidine | Famotidine | powder, for solution, oral | 50383-913ANDA |
| Trihexyphenidyl Hydrochloride | Trihexyphenidyl Hydrochloride | syrup, oral | 61748-054ANDA |
Compare
Other companies listing dorzolamide hydrochloride and timolol maleate
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- GLAND PHARMA LIMITED4 sites · 263 NDC
- Bausch & Lomb Ireland Limited4 sites · 92 NDC
- International Medication Systems, Ltd.3 sites · 2,801 NDC
- Genus Lifesciences Inc.2 sites · 46 NDC
- Bryant Ranch Prepack1 site · 4,357 NDC
Enquiry
Common questions
- Is Akorn FDA approved?
- Akorn 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 Akorn make?
- 3 products are listed under Akorn in the openFDA NDC Directory, most often as powder, for solution; solution/ drops; syrup. 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.