Data / Drug companies / Medimetriks Pharmaceuticals, Inc.
Medimetriks Pharmaceuticals, Inc.: 14 products in the FDA NDC directory, labeler code 43538
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Medimetriks Pharmaceuticals, Inc. (labeler code 43538) lists 14 products in the FDA National Drug Code Directory, covering 8 finished drugs by generic name. By type: 14 prescription drugs. Its main marketing category is generic drugs (ANDA). The newest product started marketing on June 22, 2014.
The request: Watch Medimetriks Pharmaceuticals, Inc. (FDA labeler code 43538): each new product listing and each discontinued product. $10 of work on sign-up, no card.
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- Labeler code
- 43538
- Products in commercial distribution
- 14
- Packages
- 18
- Finished drugs by generic name
- 8
- Prescription products
- 14
- Over the counter products
- 0
- Flagged as original packager
- 14 of 14 products that carry the flag
- Started marketing in the last 12 months
- 0
- Earliest marketing start
- June 11, 1963
- 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) | 10 | 71.4% |
| Other unapproved drugs | 2 | 14.3% |
| New drug applications (NDA) | 2 | 14.3% |
Products by type
| Type | Products | Share |
|---|---|---|
| Prescription drugs | 14 | 100% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Clindamycin phosphate | 3 | 31 |
| Clobetasol propionate | 2 | 40 |
| Sulfacetamide sodium and sulfur | 2 | 4 |
| Fluocinolone acetonide | 2 | 17 |
| Vancomycin hydrochloride | 2 | 39 |
| Neomycin sulfate and fluocinolone acetonide | 1 | 1 |
| Clindamycin phosphate and benzoyl peroxide | 1 | 14 |
| Ketoconazole | 1 | 35 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Aerosol, foam | 3 | 21.4% |
| Cream | 2 | 14.3% |
| Injection, powder, lyophilized, for solution | 2 | 14.3% |
| Shampoo | 1 | 7.1% |
| Kit | 1 | 7.1% |
| Gel | 1 | 7.1% |
| Ointment | 1 | 7.1% |
| Swab | 1 | 7.1% |
| Solution | 1 | 7.1% |
| Cloth | 1 | 7.1% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
| Class | Products |
|---|---|
| Corticosteroid | 5 |
| Lincosamide Antibacterial | 4 |
| Glycopeptide Antibacterial | 2 |
| Aminoglycoside Antibacterial | 1 |
| Sulfonamide Antibacterial | 1 |
| Azole Antifungal | 1 |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Clodan | 43538-950 | Shampoo | Generic drugs (ANDA) | June 22, 2014 |
| Neuac | 43538-176 | Gel | Generic drugs (ANDA) | June 15, 2014 |
| Clindacin ETZ | 43538-172 | Swab | Generic drugs (ANDA) | June 15, 2013 |
| Tovet (emollient formulation) | 43538-952 | Aerosol, foam | Generic drugs (ANDA) | February 1, 2013 |
| Synalar | 43538-910 | Ointment | New drug applications (NDA) | September 27, 2012 |
| Synalar | 43538-900 | Cream | New drug applications (NDA) | September 27, 2012 |
| Ketodan | 43538-530 | Aerosol, foam | Generic drugs (ANDA) | June 15, 2012 |
| Sumaxin CP | 43538-101 | Kit | Other unapproved drugs | August 1, 2011 |
| Clindacin P | 43538-170 | Solution | Generic drugs (ANDA) | February 20, 2011 |
| Clindacin | 43538-179 | Aerosol, foam | Generic drugs (ANDA) | March 21, 2010 |
| Sumaxin Cleansing Pads | 43538-100 | Cloth | Other unapproved drugs | January 1, 2009 |
| Vancomycin Hydrochloride | 43538-810 | Injection, powder, lyophilized, for solution | Generic drugs (ANDA) | June 30, 2008 |
| Vancomycin Hydrochloride | 43538-805 | Injection, powder, lyophilized, for solution | Generic drugs (ANDA) | June 30, 2008 |
| Neo-Synalar | 43538-940 | Cream | Generic drugs (ANDA) | June 11, 1963 |
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.