Register entry
- Registered sites
- 1
- Active NDC listings
- 9
- Labeller names
- 2
- Live patents
- 0
- Countries
- 1
- Base
- Germany
Authorisation
Registered operations
Analytical testing1Active ingredient (API) manufacture1
Sites
Registered establishments
1| Establishment | Address | Registered for | FEI / DUNS |
|---|---|---|---|
| CU Chemie Uetikon GmbH | Raiffeisenstr. 4, Lahr, 77933, Germany (DEU) | Analytical testing, Active ingredient (API) manufacture | 3002806757340717289 |
Catalogue
Drug listings by form and route
99 active NDC listings: 9 bulk ingredient. By marketing category: BULK INGREDIENT 8, BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING 1.
| Dosage form | NDCs |
|---|---|
| powder | 9 |
| Route | NDCs |
|---|
| Labeller name on the listing | NDCs |
|---|---|
| cu chemie uetikon gmbh | 8 |
| cu chemie uetikon gmbh (340717289) | 1 |
Catalogue
Marketed products
9| Brand | Generic name | Form / route | NDC |
|---|---|---|---|
| - | ESKETAMINE HYDROCHLORIDE | powder | 54382-123BULK INGREDIENT |
| - | KETAMINE HYDROCHLORIDE | powder | 54382-114BULK INGREDIENT |
| - | KETAMINE HYDROCHLORIDE | powder | 54382-128BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING |
| - | METHIMAZOLE | powder | 54382-112BULK INGREDIENT |
| - | SODIUM PHENYLACETATE | powder | 54382-124BULK INGREDIENT |
| - | SODIUM PHENYLBUTYRATE | powder | 54382-120BULK INGREDIENT |
| - | TERAZOSIN HYDROCHLORIDE ANHYDROUS | powder | 54382-116BULK INGREDIENT |
| - | TILETAMINE HYDROCHLORIDE | powder | 54382-126BULK INGREDIENT |
| - | ZOLAZEPAM HYDROCHLORIDE | powder | 54382-127BULK INGREDIENT |
Compare
Comparable companies in Germany
- Excella GmbH & Co. KG1 site · 73 NDC
- Grillo Zinc Powder GmbH1 site · 22 NDC
- Rottendorf Pharma GmbH1 site · 17 NDC
- Arevipharma GmbH1 site · 13 NDC
- Chemische Fabrik Berg GmbH1 site · 13 NDC
- Eckert & Ziegler Radiopharma GmbH1 site · 11 NDC
- Heraeus Precious Metals GmbH Co KG1 site · 10 NDC
- Solupharm Pharmazeutische Erzeugnisse GmbH1 site · 10 NDC
- BSV Bioscience GmbH1 site · 9 NDC
- Chemcon GmbH1 site · 7 NDC
Enquiry
Common questions
- Is CU Chemie Uetikon GmbH FDA approved?
- CU Chemie Uetikon GmbH holds 1 FDA-registered establishment in Germany. Registration puts a site on the FDA's register and open to inspection; it is not an approval of the company. Approvals attach to individual drug applications.
- Where are CU Chemie Uetikon GmbH's drugs manufactured?
- The FDA register lists Lahr. Registered operations: analytical testing, active ingredient (API) manufacture.
- What drugs does CU Chemie Uetikon GmbH make?
- 9 products are listed under CU Chemie Uetikon GmbH 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.