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: 2 human prescription drug, 1 human otc drug. By marketing category: BLA 2, OTC MONOGRAPH DRUG 1.
| Dosage form | NDCs |
|---|---|
| injection, powder, lyophilized, for solution | 2 |
| cream | 1 |
| Route | NDCs |
|---|---|
| intramuscular | 2 |
| topical | 1 |
| Labeller name on the listing | NDCs |
|---|---|
| hugel, inc. | 3 |
Catalogue
Marketed products
3| Brand | Generic name | Form / route | NDC |
|---|---|---|---|
| LETYBO | letibotulinumtoxinA-wlbg | injection, powder, lyophilized, for solution, intramuscular | 81165-050BLA |
| LETYBO | letibotulinumtoxinA-wlbg | injection, powder, lyophilized, for solution, intramuscular | 81165-100BLA |
| Wellage Real Hyaluronic Watery Glow Sun Screen | Avobenzone, Homosalate, Octisalate, Octocrylene | cream, topical | 81165-001OTC MONOGRAPH DRUG |
Enquiry
Common questions
- Is Hugel, Inc. FDA approved?
- Hugel, 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 Hugel, Inc. make?
- 3 products are listed under Hugel, Inc. in the openFDA NDC Directory, most often as injection, powder, lyophilized, for solution; cream. 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.