Data / Drug companies / Lannett Company, Inc.
Lannett Company, Inc.: 10 products in the FDA NDC directory, labeler code 54838
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Lannett Company, Inc. (labeler code 54838) lists 10 products in the FDA National Drug Code Directory, covering 8 finished drugs by generic name. By type: 8 prescription drugs, 2 over the counter drugs. Its main marketing category is generic drugs (ANDA). The newest product started marketing on August 17, 2015.
The request: Watch Lannett Company, Inc. (FDA labeler code 54838): each new product listing and each discontinued product. $10 of work on sign-up, no card.
SpecStream is the live web data engine for teams and agents. It reads the National Drug Code Directory that FDA publishes, and this page is that reading. Ask for the companies that make a drug, a class or a dosage form, with their headquarters, website and size added from the web, and new listings and discontinued products arrive in your sheet, CRM, Slack or agent as FDA posts them.
- Labeler code
- 54838
- Products in commercial distribution
- 10
- Packages
- 12
- Finished drugs by generic name
- 8
- Prescription products
- 8
- Over the counter products
- 2
- Flagged as original packager
- 9 of 9 products that carry the flag
- Started marketing in the last 12 months
- 0
- Earliest marketing start
- September 28, 1993
- openFDA record search
- api.fda.gov
Products by marketing category
Share of the company's products in commercial distribution.
| Marketing category | Products | Share |
|---|---|---|
| Generic drugs (ANDA) | 8 | 80% |
| Other unapproved drugs | 2 | 20% |
Products by type
| Type | Products | Share |
|---|---|---|
| Prescription drugs | 8 | 80% |
| Over the counter drugs | 2 | 20% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Loratadine | 2 | 125 |
| Hyoscyamine sulfate | 2 | 24 |
| Oxybutynin chloride | 1 | 45 |
| Aripiprazole | 1 | 49 |
| Fluoxetine hydrochloride | 1 | 44 |
| Haloperidol | 1 | 32 |
| Hydroxyzine hydrochloride | 1 | 51 |
| Doxepin hydrochloride | 1 | 45 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Solution | 6 | 60% |
| Syrup | 1 | 10% |
| Elixir | 1 | 10% |
| Liquid | 1 | 10% |
| Solution/ drops | 1 | 10% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
| Class | Products |
|---|---|
| Cholinergic Muscarinic Antagonist | 1 |
| Atypical Antipsychotic | 1 |
| Serotonin Reuptake Inhibitor | 1 |
| Typical Antipsychotic | 1 |
| Antihistamine | 1 |
| Tricyclic Antidepressant | 1 |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Aripiprazole | 54838-570 | Solution | Generic drugs (ANDA) | August 17, 2015 |
| Hydroxyzine Hydrochloride | 54838-502 | Solution | Generic drugs (ANDA) | August 21, 2013 |
| Loratadine | 54838-558 | Solution | Generic drugs (ANDA) | November 24, 2010 |
| Loratadine | 54838-554 | Solution | Generic drugs (ANDA) | November 24, 2010 |
| Fluoxetine | 54838-523 | Liquid | Generic drugs (ANDA) | August 27, 2009 |
| Doxepin Hydrochloride | 54838-512 | Solution | Generic drugs (ANDA) | December 29, 1998 |
| Hyosyne | 54838-511 | Elixir | Other unapproved drugs | November 1, 1997 |
| Hyosyne | 54838-506 | Solution/ drops | Other unapproved drugs | October 1, 1997 |
| Oxybutynin Chloride | 54838-510 | Syrup | Generic drugs (ANDA) | March 29, 1996 |
| Haloperidol | 54838-501 | Solution | Generic drugs (ANDA) | September 28, 1993 |
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.