Register entry
- Registered sites
- 0
- Active NDC listings
- 2
- Labeller names
- 2
- Live patents
- 0
- Countries
- 0
Catalogue
Drug listings by form and route
22 active NDC listings: 2 human prescription drug. By marketing category: NDA AUTHORIZED GENERIC 2.
| Dosage form | NDCs |
|---|---|
| solution | 1 |
| tablet, extended release | 1 |
| Route | NDCs |
|---|---|
| oral | 2 |
| Labeller name on the listing | NDCs |
|---|---|
| palmetto pharmaceuticals inc. | 1 |
| palmetto pharmaceuticals inc. | 1 |
Catalogue
Marketed products
2| Brand | Generic name | Form / route | NDC |
|---|---|---|---|
| Baclofen | Baclofen | solution, oral | 68134-403NDA AUTHORIZED GENERIC |
| Clonidine | Clonidine | tablet, extended release, oral | 68134-603NDA AUTHORIZED GENERIC |
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Enquiry
Common questions
- Is Palmetto Pharmaceuticals Inc. FDA approved?
- Palmetto Pharmaceuticals Inc. holds no registered establishment of its own; 2 drug products are listed under its name in the National Drug Code Directory, made at sites registered to other firms.
- What drugs does Palmetto Pharmaceuticals Inc. make?
- 2 products are listed under Palmetto Pharmaceuticals Inc. in the openFDA NDC Directory, most often as solution; tablet, extended release. 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.