Data / Drug companies / E5 Pharma, LLC
E5 Pharma, LLC: 5 products in the FDA NDC directory, labeler code 13517
E5 Pharma, LLC (labeler code 13517) lists 5 products in the FDA National Drug Code Directory, covering 3 finished drugs by generic name. By type: 5 prescription drugs. Its main marketing category is other unapproved drugs. The newest product started marketing on June 1, 2026.
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- Labeler code
- 13517
- Products in commercial distribution
- 5
- Packages
- 6
- Finished drugs by generic name
- 3
- Prescription products
- 5
- Over the counter products
- 0
- Controlled substance products
- Schedule IV 3
- Flagged as original packager
- 4 of 4 products that carry the flag
- Started marketing in the last 12 months
- 1
- Products with a marketing end date set
- 3
- Earliest marketing start
- December 11, 2019
- openFDA record search
- api.fda.gov
Products by marketing category
Share of the company's products in commercial distribution.
| Marketing category | Products | Share |
|---|---|---|
| Other unapproved drugs | 3 | 60% |
| Generic drugs (ANDA) | 2 | 40% |
Products by type
| Type | Products | Share |
|---|---|---|
| Prescription drugs | 5 | 100% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Phenobarbital | 3 | 25 |
| Nitazoxanide | 1 | 4 |
| Diazoxide | 1 | 3 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet | 4 | 80% |
| Suspension | 1 | 20% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
| Class | Products |
|---|---|
| Antiprotozoal | 1 |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Nitazoxanide | 13517-135 | Tablet | Generic drugs (ANDA) | June 1, 2026 |
| Phenobarbital | 13517-694 | Tablet | Other unapproved drugs | November 30, 2022 |
| Phenobarbital | 13517-693 | Tablet | Other unapproved drugs | November 30, 2022 |
| Phenobarbital | 13517-692 | Tablet | Other unapproved drugs | November 30, 2022 |
| Diazoxide | 13517-100 | Suspension | Generic drugs (ANDA) | December 11, 2019 |
Updated November 6, 2026. Read from US Food and Drug Administration, National Drug Code Directory (openFDA). 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.