Data / Drug companies / Marlex Pharmaceuticals, Inc.
Marlex Pharmaceuticals, Inc.: 110 products in the FDA NDC directory, labeler code 10135
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Marlex Pharmaceuticals, Inc. (labeler code 10135) lists 110 products in the FDA National Drug Code Directory, covering 54 finished drugs by generic name. By type: 95 prescription drugs, 15 over the counter drugs. Its main marketing category is generic drugs (ANDA). The newest product started marketing on September 1, 2026.
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- Labeler code
- 10135
- Products in commercial distribution
- 110
- Packages
- 202
- Finished drugs by generic name
- 54
- Prescription products
- 95
- Over the counter products
- 15
- Controlled substance products
- Schedule V 4
- Flagged as original packager
- 61 of 61 products that carry the flag
- Started marketing in the last 12 months
- 10
- Earliest marketing start
- July 29, 1976
- 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) | 90 | 81.8% |
| Over the counter monograph drugs | 13 | 11.8% |
| New drug applications (NDA) | 5 | 4.5% |
| Other unapproved drugs | 2 | 1.8% |
Products by type
| Type | Products | Share |
|---|---|---|
| Prescription drugs | 95 | 86.4% |
| Over the counter drugs | 15 | 13.6% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet | 55 | 50% |
| Tablet, film coated | 29 | 26.4% |
| Capsule | 5 | 4.5% |
| Tablet, extended release | 4 | 3.6% |
| Solution | 4 | 3.6% |
| Capsule, extended release | 3 | 2.7% |
| Cream | 2 | 1.8% |
| Capsule, gelatin coated | 1 | 0.9% |
| Ointment | 1 | 0.9% |
| Powder | 1 | 0.9% |
| Suppository | 1 | 0.9% |
| Suspension | 1 | 0.9% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Metformin hydrochloride | 10135-824 | Tablet, extended release | Generic drugs (ANDA) | September 1, 2026 |
| Metformin hydrochloride | 10135-823 | Tablet, extended release | Generic drugs (ANDA) | September 1, 2026 |
| Ramelteon | 10135-838 | Tablet, film coated | Generic drugs (ANDA) | July 1, 2026 |
| Furosemide | 10135-834 | Tablet | New drug applications (NDA) | March 1, 2026 |
| Furosemide | 10135-833 | Tablet | New drug applications (NDA) | March 1, 2026 |
| Furosemide | 10135-832 | Tablet | New drug applications (NDA) | March 1, 2026 |
| Acetazolamide | 10135-831 | Tablet | Generic drugs (ANDA) | February 1, 2026 |
| Acetazolamide | 10135-830 | Tablet | Generic drugs (ANDA) | February 1, 2026 |
| Acetaminophen | 10135-829 | Tablet | Over the counter monograph drugs | February 1, 2026 |
| Acetaminophen 325mg | 10135-828 | Tablet | Over the counter monograph drugs | February 1, 2026 |
| Venlafaxine hydrochloride | 10135-827 | Capsule, extended release | Generic drugs (ANDA) | August 1, 2025 |
| Venlafaxine hydrochloride | 10135-826 | Capsule, extended release | Generic drugs (ANDA) | August 1, 2025 |
| Venlafaxine hydrochloride | 10135-825 | Capsule, extended release | Generic drugs (ANDA) | August 1, 2025 |
| Potassium Chloride for Oral Solution | 10135-820 | Solution | Generic drugs (ANDA) | August 1, 2025 |
| Potassium Chloride for Oral Solution | 10135-819 | Solution | Generic drugs (ANDA) | August 1, 2025 |
| Potassium Chloride for Oral Solution | 10135-807 | Powder, for solution | Generic drugs (ANDA) | August 1, 2025 |
| Desvenlafaxine | 10135-822 | Tablet, extended release | Generic drugs (ANDA) | July 1, 2025 |
| Desvenlafaxine | 10135-821 | Tablet, extended release | Generic drugs (ANDA) | July 1, 2025 |
| Lacosamide | 10135-802 | Tablet, film coated | Generic drugs (ANDA) | July 1, 2025 |
| Lacosamide | 10135-801 | Tablet, film coated | Generic drugs (ANDA) | July 1, 2025 |
| Lacosamide | 10135-800 | Tablet, film coated | Generic drugs (ANDA) | July 1, 2025 |
| Lacosamide | 10135-799 | Tablet, film coated | Generic drugs (ANDA) | May 23, 2025 |
| Oxcarbazepine | 10135-798 | Suspension | Generic drugs (ANDA) | May 1, 2025 |
| Benztropine mesylate | 10135-815 | Tablet | Generic drugs (ANDA) | March 1, 2025 |
| Benztropine mesylate | 10135-814 | Tablet | Generic drugs (ANDA) | March 1, 2025 |
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.