Data / Drug companies / Cu Chemie Uetikon GmbH
Cu Chemie Uetikon GmbH: 9 products in the FDA NDC directory, labeler code 54382
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Cu Chemie Uetikon GmbH (labeler code 54382) lists 9 products in the FDA National Drug Code Directory. By type: 9 bulk ingredients. Its main marketing category is bulk ingredients. The newest product started marketing on September 30, 2011.
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- Labeler code
- 54382
- Products in commercial distribution
- 9
- Packages
- 9
- Finished drugs by generic name
- 0
- Prescription products
- 0
- Over the counter products
- 0
- Controlled substance products
- Schedule III 5
- Started marketing in the last 12 months
- 0
- Earliest marketing start
- February 8, 1989
- openFDA record search
- api.fda.gov
Products by marketing category
Share of the company's products in commercial distribution.
| Marketing category | Products | Share |
|---|---|---|
| Bulk ingredients | 8 | 88.9% |
| Bulk ingredients for compounding | 1 | 11.1% |
Products by type
| Type | Products | Share |
|---|---|---|
| Bulk ingredients | 9 | 100% |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Powder | 9 | 100% |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Zolazepam hydrochloride | 54382-127 | Powder | Bulk ingredients | September 30, 2011 |
| Tiletamine hydrochloride | 54382-126 | Powder | Bulk ingredients | July 15, 2011 |
| Sodium phenylacetate | 54382-124 | Powder | Bulk ingredients | September 16, 2002 |
| Esketamine hydrochloride | 54382-123 | Powder | Bulk ingredients | July 11, 2001 |
| Sodium phenylbutyrate | 54382-120 | Powder | Bulk ingredients | June 10, 1997 |
| Terazosin hydrochloride anhydrous | 54382-116 | Powder | Bulk ingredients | August 23, 1991 |
| Ketamine hydrochloride | 54382-128 | Powder | Bulk ingredients for compounding | August 2, 1989 |
| Ketamine hydrochloride | 54382-114 | Powder | Bulk ingredients | February 8, 1989 |
| Methimazole | 54382-112 | Powder | Bulk ingredients | February 8, 1989 |
CC0 1.0 public domain dedication (openFDA). Counts are products in the FDA National Drug Code Directory on November 6, 2026: 138,262 products in commercial distribution, meaning without a marketing end date in the past. A company is a labeler code; one company can hold several codes, and the directory carries no address. Inclusion in the directory is not FDA approval, and the marketing category says under which kind of application or rule a product is sold. This page uses openFDA data and is not endorsed or certified by FDA. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.