Data / Drug companies / Gendose Pharmaceuticals, LLC
Gendose Pharmaceuticals, LLC: 11 products in the FDA NDC directory, labeler code 77333
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Gendose Pharmaceuticals, LLC (labeler code 77333) lists 11 products in the FDA National Drug Code Directory, covering 7 finished drugs by generic name. By type: 11 over the counter drugs. Its main marketing category is over the counter monograph drugs. The newest product started marketing on May 15, 2026.
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- Labeler code
- 77333
- Products in commercial distribution
- 11
- Packages
- 11
- Finished drugs by generic name
- 7
- Prescription products
- 0
- Over the counter products
- 11
- Flagged as original packager
- 7 of 7 products that carry the flag
- Started marketing in the last 12 months
- 6
- Earliest marketing start
- September 2, 2022
- 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 | 11 | 100% |
Products by type
| Type | Products | Share |
|---|---|---|
| Over the counter drugs | 11 | 100% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Aspirin | 4 | 134 |
| Diphenhydramine hcl | 2 | 99 |
| Guaifenesin | 1 | 123 |
| Calcium polycarbophil | 1 | 33 |
| Sodium bicarbonate | 1 | 51 |
| Simethicone | 1 | 86 |
| Sodium chloride | 1 | 71 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet | 4 | 36.4% |
| Capsule | 2 | 18.2% |
| Tablet, delayed release | 2 | 18.2% |
| Tablet, chewable | 2 | 18.2% |
| Tablet, film coated | 1 | 9.1% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
| Class | Products |
|---|---|
| Nonsteroidal Anti-inflammatory Drug | 4 |
| Platelet Aggregation Inhibitor | 4 |
| Histamine-1 Receptor Antagonist | 2 |
| Expectorant | 1 |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Antihistamine | 77333-231 | Capsule | Over the counter monograph drugs | May 15, 2026 |
| Antihistamine | 77333-227 | Capsule | Over the counter monograph drugs | May 15, 2026 |
| Aspirin | 77333-050 | Tablet, film coated | Over the counter monograph drugs | May 15, 2026 |
| Aspirin Enteric Coated, Regular Strength | 77333-035 | Tablet, delayed release | Over the counter monograph drugs | May 15, 2026 |
| Sodium chloride 1 gram | 77333-846 | Tablet | Over the counter monograph drugs | May 1, 2026 |
| Sodium Bicarbonate 10 gr. (650 mg) | 77333-829 | Tablet | Over the counter monograph drugs | May 1, 2026 |
| Aspirin 81mg | 77333-049 | Tablet, chewable | Over the counter monograph drugs | May 1, 2025 |
| Aspirin 81mg Enteric Coated | 77333-031 | Tablet, delayed release | Over the counter monograph drugs | May 1, 2025 |
| Simethicone 80mg | 77333-812 | Tablet, chewable | Over the counter monograph drugs | September 2, 2022 |
| Guaifenesin 400mg caplets | 77333-360 | Tablet | Over the counter monograph drugs | September 2, 2022 |
| Fiber laxative caplets | 77333-120 | Tablet | Over the counter monograph drugs | September 2, 2022 |
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.