Register entry
- Registered sites
- 0
- Active NDC listings
- 17
- Live patents
- 0
- Countries
- 0
Catalogue
Drug listings by form and route
1717 active NDC listings: 17 bulk ingredient. By marketing category: BULK INGREDIENT 17.
| Dosage form | NDCs |
|---|---|
| powder | 17 |
| Route | NDCs |
|---|
| Labeller name on the listing | NDCs |
|---|---|
| uquifa spain | 17 |
Catalogue
Marketed products
17| Brand | Generic name | Form / route | NDC |
|---|---|---|---|
| - | Allopurinol | powder | 49711-0113BULK INGREDIENT |
| - | Duloxetine HCl | powder | 49711-1507BULK INGREDIENT |
| - | Emtricitabine | powder | 49711-1516BULK INGREDIENT |
| - | Esomeprazole Magnesium Dihydrate | powder | 49711-0118BULK INGREDIENT |
| - | Esomeprazole Sodium | powder | 49711-0119BULK INGREDIENT |
| - | Famotidine | powder | 49711-0098BULK INGREDIENT |
| - | Hexyl Aminolevulinate Hydrochloride | powder | 49711-1510BULK INGREDIENT |
| - | Hydroxyzine Pamoate | powder | 49711-1508BULK INGREDIENT |
| - | Lansoprazole | powder | 49711-0110BULK INGREDIENT |
| - | Linezolid | powder | 49711-0121BULK INGREDIENT |
| - | Memantine Hydrochloride | powder | 49711-1515BULK INGREDIENT |
| - | Mivacurium Chloride 4% | powder | 49711-1503BULK INGREDIENT |
| - | Nimodipine Micronized | powder | 49711-0104BULK INGREDIENT |
| - | Omperazole Micronized | powder | 49711-0109BULK INGREDIENT |
| - | Quetiapine Fumarate | powder | 49711-1506BULK INGREDIENT |
| - | Ranitidine Hydrochloride | powder | 49711-0107BULK INGREDIENT |
| - | Robenidine Hydrochloride | powder | 49711-0106BULK INGREDIENT |
Compare
Other companies listing allopurinol
- Cardinal Health 418, Inc.34 sites · 833 NDC
- Sun Pharmaceutical Industries Limited13 sites · 918 NDC
- Zydus Lifesciences Limited12 sites · 717 NDC
- Ipca Laboratories Limited7 sites · 77 NDC
- Indoco Remedies Limited7 sites · 58 NDC
- Aurobindo Pharma Limited6 sites · 1,453 NDC
- Fresenius Kabi USA, LLC6 sites · 561 NDC
- Spectrum Pharmaceuticals, Inc.6 sites · 240 NDC
- Pharma Packaging Solutions, LLC dba Tjoapack, LLC5 sites · 667 NDC
- Unichem Laboratories Limited, India5 sites · 272 NDC
Enquiry
Common questions
- Is Uquifa Spain FDA approved?
- Uquifa Spain holds no registered establishment of its own; 17 drug products are listed under its name in the National Drug Code Directory, made at sites registered to other firms.
- What drugs does Uquifa Spain make?
- 17 products are listed under Uquifa Spain in the openFDA NDC Directory, most often as powder. 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.