Data / Drug companies / Prestige Brands Holdings, Inc.
Prestige Brands Holdings, Inc.: 7 products in the FDA NDC directory, labeler code 52183
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Prestige Brands Holdings, Inc. (labeler code 52183) lists 7 products in the FDA National Drug Code Directory, covering 5 finished drugs by generic name. By type: 7 over the counter drugs. Its main marketing category is over the counter monograph drugs. The newest product started marketing on February 1, 2023.
The request: Watch Prestige Brands Holdings, Inc. (FDA labeler code 52183): 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
- 52183
- Products in commercial distribution
- 7
- Packages
- 12
- Finished drugs by generic name
- 5
- Prescription products
- 0
- Over the counter products
- 7
- Flagged as original packager
- 7 of 7 products that carry the flag
- Started marketing in the last 12 months
- 0
- Products with a marketing end date set
- 1
- Earliest marketing start
- October 29, 2009
- openFDA record search
- api.fda.gov
Products by marketing category
Share of the company's products in commercial distribution.
| Marketing category | Products | Share |
|---|---|---|
| Over the counter monograph drugs | 5 | 71.4% |
| Generic drugs (ANDA) | 1 | 14.3% |
| New drug applications (NDA) | 1 | 14.3% |
Products by type
| Type | Products | Share |
|---|---|---|
| Over the counter drugs | 7 | 100% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Pectin | 3 | 14 |
| Pectin and menthol | 1 | 1 |
| Menthol | 1 | 263 |
| Cromolyn sodium | 1 | 11 |
| Cimetidine | 1 | 19 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Lozenge | 5 | 71.4% |
| Spray, metered | 1 | 14.3% |
| Tablet | 1 | 14.3% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
| Class | Products |
|---|---|
| Mast Cell Stabilizer | 1 |
| Histamine-2 Receptor Antagonist | 1 |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Tagamet | 52183-223 | Tablet | New drug applications (NDA) | February 1, 2023 |
| Ludens Dual Relief | 52183-227 | Lozenge | Over the counter monograph drugs | June 15, 2018 |
| Ludens sugar free wild cherry throat | 52183-249 | Lozenge | Over the counter monograph drugs | July 12, 2010 |
| Ludens Honey Licorice Throat Drops | 52183-255 | Lozenge | Over the counter monograph drugs | October 29, 2009 |
| Ludens Wild Cherry Throat Drops | 52183-229 | Lozenge | Over the counter monograph drugs | October 29, 2009 |
| Ludens Watermelon Throat Drops | 52183-202 | Lozenge | Over the counter monograph drugs | October 29, 2009 |
| NasalCrom | 52183-199 | Spray, metered | Generic drugs (ANDA) | October 29, 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.