Data / Drug companies / Solupharm Pharmazeutische Erzeugnisse GmbH
Solupharm Pharmazeutische Erzeugnisse GmbH: 10 products in the FDA NDC directory, labeler code 55579
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Solupharm Pharmazeutische Erzeugnisse GmbH (labeler code 55579) lists 10 products in the FDA National Drug Code Directory, covering 4 finished drugs by generic name. By type: 5 drugs for further processing, 5 prescription drugs. Its main marketing category is drugs for further processing. The newest product started marketing on July 28, 2026.
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- Labeler code
- 55579
- Products in commercial distribution
- 10
- Packages
- 11
- Finished drugs by generic name
- 4
- Prescription products
- 5
- Over the counter products
- 0
- Flagged as original packager
- 4 of 4 products that carry the flag
- Started marketing in the last 12 months
- 2
- Earliest marketing start
- April 24, 2008
- openFDA record search
- api.fda.gov
Products by marketing category
Share of the company's products in commercial distribution.
| Marketing category | Products | Share |
|---|---|---|
| Drugs for further processing | 5 | 50% |
| Generic drugs (ANDA) | 5 | 50% |
Products by type
| Type | Products | Share |
|---|---|---|
| Drugs for further processing | 5 | 50% |
| Prescription drugs | 5 | 50% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Acetaminophen | 2 | 214 |
| Alcohol | 1 | 293 |
| Sugammadex sodium | 1 | 5 |
| Sugammadex | 1 | 22 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Injection, solution | 5 | 50% |
| Liquid | 3 | 30% |
| Injection | 2 | 20% |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Sugammadex | 55579-893 | Injection, solution | Generic drugs (ANDA) | July 28, 2026 |
| Sugammadex | 55579-892 | Injection, solution | Generic drugs (ANDA) | July 28, 2026 |
| Dehydrated Alcohol | 55579-306 | Injection | Generic drugs (ANDA) | January 8, 2025 |
| Acetaminophen | 55579-405 | Injection, solution | Generic drugs (ANDA) | December 7, 2020 |
| Acetaminophen | 55579-110 | Injection | Generic drugs (ANDA) | December 7, 2020 |
| Bupivacaine hydrochloride | 55579-397 | Liquid | Drugs for further processing | April 2, 2019 |
| Lidocaine hydrochloride | 55579-939 | Liquid | Drugs for further processing | August 3, 2018 |
| Sodium chloride | 55579-937 | Liquid | Drugs for further processing | August 9, 2016 |
| Promethazine hydrochloride | 55579-402 | Injection, solution | Drugs for further processing | April 24, 2008 |
| Promethazine hydrochloride | 55579-401 | Injection, solution | Drugs for further processing | April 24, 2008 |
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.