Data / Drug companies / Elementis Pharma Gmbh
Elementis Pharma Gmbh: 14 products in the FDA NDC directory, labeler code 55603
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Elementis Pharma Gmbh (labeler code 55603) lists 14 products in the FDA National Drug Code Directory. By type: 14 bulk ingredients. Its main marketing category is bulk ingredients. The newest product started marketing on November 12, 2013.
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- Labeler code
- 55603
- Products in commercial distribution
- 14
- Packages
- 14
- Finished drugs by generic name
- 0
- Prescription products
- 0
- Over the counter products
- 0
- Started marketing in the last 12 months
- 0
- Earliest marketing start
- August 5, 2010
- 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 | 14 | 100% |
Products by type
| Type | Products | Share |
|---|---|---|
| Bulk ingredients | 14 | 100% |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Powder | 8 | 57.1% |
| Paste | 4 | 28.6% |
| Gel | 2 | 14.3% |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Sucralfate | 55603-805 | Powder | Bulk ingredients | November 12, 2013 |
| Magaldrate | 55603-170 | Powder | Bulk ingredients | November 12, 2013 |
| Hydrotalcite | 55603-159 | Powder | Bulk ingredients | November 12, 2013 |
| Magaldrate | 55603-073 | Gel | Bulk ingredients | November 12, 2013 |
| Aluminum hydroxide wet gel | 55603-057 | Gel | Bulk ingredients | November 11, 2013 |
| Sodium monofluorophosphate | 55603-240 | Powder | Bulk ingredients | March 28, 2011 |
| Aluminum hydroxide | 55603-671 | Paste | Bulk ingredients | September 22, 2010 |
| Magnesium hydroxide | 55603-661 | Paste | Bulk ingredients | September 22, 2010 |
| Sucralfate | 55603-611 | Paste | Bulk ingredients | September 22, 2010 |
| Sucralfate | 55603-225 | Powder | Bulk ingredients | September 22, 2010 |
| Sucralfate | 55603-215 | Powder | Bulk ingredients | September 22, 2010 |
| Aluminum hydroxide | 55603-211 | Powder | Bulk ingredients | September 22, 2010 |
| Dihydroxyaluminum sodium carbonate | 55603-265 | Paste | Bulk ingredients | August 13, 2010 |
| Aluminum phosphate | 55603-111 | Powder | Bulk ingredients | August 5, 2010 |
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.