Data / Drug companies / Magno-Humphries, Inc.
Magno-Humphries, Inc.: 18 products in the FDA NDC directory, labeler code 54257
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Magno-Humphries, Inc. (labeler code 54257) lists 18 products in the FDA National Drug Code Directory, covering 13 finished drugs by generic name. By type: 18 over the counter drugs. Its main marketing category is over the counter monograph drugs. The newest product started marketing on July 25, 2022.
The request: Watch Magno-Humphries, Inc. (FDA labeler code 54257): each new product listing and each discontinued product. $10 of work on sign-up, no card.
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- Labeler code
- 54257
- Products in commercial distribution
- 18
- Packages
- 20
- Finished drugs by generic name
- 13
- Prescription products
- 0
- Over the counter products
- 18
- Flagged as original packager
- 18 of 18 products that carry the flag
- Started marketing in the last 12 months
- 0
- Earliest marketing start
- April 26, 2016
- 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 | 13 | 72.2% |
| Generic drugs (ANDA) | 5 | 27.8% |
Products by type
| Type | Products | Share |
|---|---|---|
| Over the counter drugs | 18 | 100% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Acetaminophen | 3 | 214 |
| Docusate sodium | 2 | 79 |
| Famotidine | 2 | 138 |
| Calcium polycarbophil | 2 | 33 |
| Acetaminophen, diphenhydramine hydrochloride | 1 | 14 |
| Cetirizine hydrochloride | 1 | 119 |
| Aspirin | 1 | 134 |
| Fexofenadine hydrochloride | 1 | 65 |
| Dextromethorphan hydrobromide, guaifenesin | 1 | 49 |
| Docusate sodium, sennosides | 1 | 18 |
| Sennosides | 1 | 65 |
| Guaifenesin | 1 | 123 |
| Acetaminophen, aspirin, caffeine | 1 | 48 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet | 14 | 77.8% |
| Capsule, gelatin coated | 2 | 11.1% |
| Tablet, film coated | 2 | 11.1% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Fiber laxative | 54257-479 | Tablet | Over the counter monograph drugs | July 25, 2022 |
| Allergy Relief | 54257-170 | Tablet | Generic drugs (ANDA) | March 25, 2021 |
| Stool Softener Docusate Sodium | 54257-902 | Capsule, gelatin coated | Over the counter monograph drugs | January 24, 2020 |
| Extraprin | 54257-858 | Tablet | Over the counter monograph drugs | January 24, 2020 |
| Mucosa Guifenesin | 54257-776 | Tablet | Over the counter monograph drugs | January 24, 2020 |
| Acetaminophen Regular Strength | 54257-720 | Tablet | Over the counter monograph drugs | January 24, 2020 |
| Sennosides Natural Laxative | 54257-679 | Tablet | Over the counter monograph drugs | January 24, 2020 |
| Acetaminophen Extended-Release | 54257-573 | Tablet | Generic drugs (ANDA) | January 24, 2020 |
| Pain Reliever | 54257-473 | Tablet | Over the counter monograph drugs | January 24, 2020 |
| Fiber Laxative | 54257-379 | Tablet | Over the counter monograph drugs | January 24, 2020 |
| Pain Reliever PM | 54257-278 | Tablet | Over the counter monograph drugs | January 24, 2020 |
| Allergy Relief | 54257-270 | Tablet | Generic drugs (ANDA) | January 24, 2020 |
| Senna S | 54257-089 | Tablet | Over the counter monograph drugs | January 24, 2020 |
| Enteric coated aspirin | 54257-274 | Tablet | Over the counter monograph drugs | January 16, 2020 |
| Stool Softener Docusate Sodium | 54257-902 | Capsule, gelatin coated | Over the counter monograph drugs | April 4, 2017 |
| Mucosa DM | 54257-277 | Tablet | Over the counter monograph drugs | April 4, 2017 |
| Famotidine | 54257-802 | Tablet, film coated | Generic drugs (ANDA) | April 26, 2016 |
| Famotidine | 54257-180 | Tablet, film coated | Generic drugs (ANDA) | April 26, 2016 |
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.