Data / Drug companies / Liebel-Flarsheim Company LLC
Liebel-Flarsheim Company LLC: 10 products in the FDA NDC directory, labeler code 0019
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Liebel-Flarsheim Company LLC (labeler code 0019) lists 10 products in the FDA National Drug Code Directory, covering 4 finished drugs by generic name. By type: 10 prescription drugs. Its main marketing category is new drug applications (NDA). The newest product started marketing on November 18, 2020.
The request: Watch Liebel-Flarsheim Company LLC (FDA labeler code 0019): each new product listing and each discontinued product. $10 of work on sign-up, no card.
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- Labeler code
- 0019
- Products in commercial distribution
- 10
- Packages
- 59
- Finished drugs by generic name
- 4
- Prescription products
- 10
- Over the counter products
- 0
- Flagged as original packager
- 10 of 10 products that carry the flag
- Started marketing in the last 12 months
- 0
- Earliest marketing start
- August 31, 2009
- openFDA record search
- api.fda.gov
Products by marketing category
Share of the company's products in commercial distribution.
| Marketing category | Products | Share |
|---|---|---|
| New drug applications (NDA) | 9 | 90% |
| Generic drugs (ANDA) | 1 | 10% |
Products by type
| Type | Products | Share |
|---|---|---|
| Prescription drugs | 10 | 100% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Ioversol | 7 | 1 |
| Sodium chloride | 1 | 71 |
| Iothalamate meglumine | 1 | 1 |
| Diatrizoate meglumine and diatrizoate sodium | 1 | 4 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Injection | 9 | 90% |
| Solution | 1 | 10% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
| Class | Products |
|---|---|
| Radiographic Contrast Agent | 9 |
| Osmotic Laxative | 1 |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Optiray 350 | 0019-1333 | Injection | New drug applications (NDA) | November 18, 2020 |
| Optiray 320 | 0019-1323 | Injection | New drug applications (NDA) | November 18, 2020 |
| Sodium chloride | 0019-1188 | Injection | New drug applications (NDA) | September 1, 2012 |
| Optiray 350 | 0019-1333 | Injection | New drug applications (NDA) | March 4, 2012 |
| Optiray 300 | 0019-1332 | Injection | New drug applications (NDA) | March 4, 2012 |
| Optiray 320 | 0019-1323 | Injection | New drug applications (NDA) | March 4, 2012 |
| Optiray 350 | 0019-1333 | Injection | New drug applications (NDA) | October 17, 2011 |
| Optiray 320 | 0019-1323 | Injection | New drug applications (NDA) | October 17, 2011 |
| Cysto-Conray II | 0019-0862 | Injection | New drug applications (NDA) | October 8, 2010 |
| Md gastroview | 0019-4816 | Solution | Generic drugs (ANDA) | August 31, 2009 |
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.