Data / Drug companies / Medsource Pharmaceuticals
Medsource Pharmaceuticals: 20 products in the FDA NDC directory, labeler code 45865
Medsource Pharmaceuticals (labeler code 45865) lists 20 products in the FDA National Drug Code Directory, covering 17 finished drugs by generic name. By type: 20 prescription drugs. Its main marketing category is generic drugs (ANDA). The newest product started marketing on September 15, 2022.
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- Labeler code
- 45865
- Products in commercial distribution
- 20
- Packages
- 36
- Finished drugs by generic name
- 17
- Prescription products
- 20
- Over the counter products
- 0
- Controlled substance products
- Schedule IV 4
- Started marketing in the last 12 months
- 0
- Earliest marketing start
- May 1, 2003
- 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) | 20 | 100% |
Products by type
| Type | Products | Share |
|---|---|---|
| Prescription drugs | 20 | 100% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Gabapentin | 2 | 91 |
| Amoxicillin and clavulanate potassium | 2 | 35 |
| Trazodone hydrochloride | 2 | 39 |
| Esomeprazole magnesium | 1 | 77 |
| Cyclobenzaprine hydrochloride | 1 | 61 |
| Fluoxetine hydrochloride | 1 | 44 |
| Etodolac | 1 | 31 |
| Diclofenac sodium topical | 1 | 11 |
| Methocarbamol | 1 | 67 |
| Tramadol hydrochloride and acetaminophen | 1 | 13 |
| Carisoprodol | 1 | 28 |
| Naproxen | 1 | 58 |
| Tramadol hydrochloride | 1 | 44 |
| Celecoxib | 1 | 63 |
| Hydroxyzine hydrochloride | 1 | 51 |
| Alprazolam | 1 | 37 |
| Prednisone | 1 | 49 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet | 8 | 40% |
| Tablet, film coated | 5 | 25% |
| Capsule | 4 | 20% |
| Capsule, delayed release | 1 | 5% |
| Gel | 1 | 5% |
| Tablet, extended release | 1 | 5% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Diclofenac Sodium | 45865-260 | Gel | Generic drugs (ANDA) | September 15, 2022 |
| Prednisone | 45865-884 | Tablet | Generic drugs (ANDA) | September 1, 2021 |
| Celecoxib | 45865-234 | Capsule | Generic drugs (ANDA) | December 3, 2020 |
| Naproxen | 45865-238 | Tablet | Generic drugs (ANDA) | March 1, 2020 |
| Carisoprodol | 45865-233 | Tablet | Generic drugs (ANDA) | January 20, 2020 |
| Methocarbamol | 45865-242 | Tablet | Generic drugs (ANDA) | August 15, 2019 |
| Gabapentin | 45865-216 | Capsule | Generic drugs (ANDA) | May 14, 2018 |
| Trazodone Hydrochloride | 45865-167 | Tablet | Generic drugs (ANDA) | December 11, 2017 |
| Tramadol Hydrochloride and Acetaminophen | 45865-170 | Tablet, film coated | Generic drugs (ANDA) | March 22, 2017 |
| Amoxicillin and Clavulanate Potassium | 45865-230 | Tablet, film coated | Generic drugs (ANDA) | March 1, 2017 |
| Amoxicillin and clavulanate potassium | 45865-227 | Tablet, film coated | Generic drugs (ANDA) | March 1, 2017 |
| Gabapentin | 45865-194 | Capsule | Generic drugs (ANDA) | February 18, 2016 |
| Esomeprazole Magnesium | 45865-163 | Capsule, delayed release | Generic drugs (ANDA) | December 10, 2015 |
| Alprazolam | 45865-257 | Tablet | Generic drugs (ANDA) | July 31, 2015 |
| Fluoxetine | 45865-174 | Capsule | Generic drugs (ANDA) | March 16, 2015 |
| Hydroxyzine hydrochloride | 45865-675 | Tablet | Generic drugs (ANDA) | August 20, 2014 |
| Tramadol hydrochloride | 45865-184 | Tablet, extended release | Generic drugs (ANDA) | August 19, 2014 |
| Trazodone Hydrochloride | 45865-505 | Tablet | Generic drugs (ANDA) | November 27, 2013 |
| Cyclobenzaprine Hydrochloride | 45865-244 | Tablet, film coated | Generic drugs (ANDA) | September 26, 2008 |
| Etodolac | 45865-206 | Tablet, film coated | Generic drugs (ANDA) | May 1, 2003 |
Updated November 6, 2026. Read from US Food and Drug Administration, National Drug Code Directory (openFDA). 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.