Register entry
- Registered sites
- 0
- Active NDC listings
- 2
- Live patents
- 0
- Countries
- 0
Catalogue
Drug listings by form and route
22 active NDC listings: 2 human prescription drug. By marketing category: ANDA 2.
| Dosage form | NDCs |
|---|---|
| tablet, film coated | 2 |
| Route | NDCs |
|---|---|
| oral | 2 |
| Labeller name on the listing | NDCs |
|---|---|
| pharmaka generics inc. | 2 |
Catalogue
Marketed products
2| Brand | Generic name | Form / route | NDC |
|---|---|---|---|
| Tetracycline Hydrochloride | Tetracycline Hydrochloride | tablet, film coated, oral | 82644-087ANDA |
| Tetracycline Hydrochloride | Tetracycline Hydrochloride | tablet, film coated, oral | 82644-870ANDA |
Compare
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Enquiry
Common questions
- Is Pharmaka Generics Inc. FDA approved?
- Pharmaka Generics 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 Pharmaka Generics Inc. make?
- 2 products are listed under Pharmaka Generics Inc. in the openFDA NDC Directory, most often as tablet, film coated. 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.