Data / Drug companies / Xenex Laboratories Inc
Xenex Laboratories Inc: 38 products in the FDA NDC directory, labeler code 68981
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Xenex Laboratories Inc (labeler code 68981) lists 38 products in the FDA National Drug Code Directory, covering 1 finished drug by generic name. By type: 37 bulk ingredients, 1 over the counter drugs. Its main marketing category is bulk ingredients. The newest product started marketing on October 30, 2024.
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- Labeler code
- 68981
- Products in commercial distribution
- 38
- Packages
- 132
- Finished drugs by generic name
- 1
- Prescription products
- 0
- Over the counter products
- 1
- Flagged as original packager
- 1 of 1 products that carry the flag
- Started marketing in the last 12 months
- 0
- Earliest marketing start
- August 1, 2020
- openFDA record search
- api.fda.gov
Products by marketing category
Share of the company's products in commercial distribution.
| Marketing category | Products | Share |
|---|---|---|
| Bulk ingredients | 37 | 97.4% |
| Over the counter monograph drugs | 1 | 2.6% |
Products by type
| Type | Products | Share |
|---|---|---|
| Bulk ingredients | 37 | 97.4% |
| Over the counter drugs | 1 | 2.6% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Menthol, capsaicin | 1 | 8 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Powder | 37 | 97.4% |
| Cream | 1 | 2.6% |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Xencare inflamax natural topical pain | 68981-900 | Cream | Over the counter monograph drugs | October 30, 2024 |
| Phenazopyridine hcl | 68981-046 | Powder | Bulk ingredients | April 21, 2021 |
| Clotrimazole | 68981-045 | Powder | Bulk ingredients | April 21, 2021 |
| Fluoxetine hydrochloride | 68981-044 | Powder | Bulk ingredients | April 21, 2021 |
| Tadalafil | 68981-043 | Powder | Bulk ingredients | April 21, 2021 |
| Piroxicam | 68981-041 | Powder | Bulk ingredients | April 21, 2021 |
| Nifedipine | 68981-039 | Powder | Bulk ingredients | April 21, 2021 |
| Naproxen base | 68981-038 | Powder | Bulk ingredients | April 21, 2021 |
| Naltrexone hydrochloride | 68981-037 | Powder | Bulk ingredients | April 21, 2021 |
| Minoxidil | 68981-036 | Powder | Bulk ingredients | April 21, 2021 |
| Miconazole nitrate | 68981-035 | Powder | Bulk ingredients | April 21, 2021 |
| Metronidazole | 68981-034 | Powder | Bulk ingredients | April 21, 2021 |
| Ketoprofen | 68981-031 | Powder | Bulk ingredients | April 21, 2021 |
| Clonidine hydrochloride | 68981-029 | Powder | Bulk ingredients | April 21, 2021 |
| Clobetasol propionate micronized | 68981-027 | Powder | Bulk ingredients | April 21, 2021 |
| Clindamycin phosphate | 68981-026 | Powder | Bulk ingredients | April 21, 2021 |
| Meclizine hydrochloride | 68981-024 | Powder | Bulk ingredients | April 21, 2021 |
| Ketoconazole | 68981-023 | Powder | Bulk ingredients | April 21, 2021 |
| Loperamide hydrochloride | 68981-022 | Powder | Bulk ingredients | April 21, 2021 |
| Finasteride | 68981-021 | Powder | Bulk ingredients | April 21, 2021 |
| Erythromycin | 68981-019 | Powder | Bulk ingredients | April 21, 2021 |
| Diltiazem hydrochloride | 68981-018 | Powder | Bulk ingredients | April 21, 2021 |
| Budesonide | 68981-017 | Powder | Bulk ingredients | April 21, 2021 |
| Amlodipine besylate | 68981-016 | Powder | Bulk ingredients | April 21, 2021 |
| Amitriptyline hydrochloride | 68981-015 | Powder | Bulk ingredients | April 21, 2021 |
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.