Data / Drug companies / Almatica Pharma LLC
Almatica Pharma LLC: 24 products in the FDA NDC directory, labeler code 52427
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Almatica Pharma LLC (labeler code 52427) lists 24 products in the FDA National Drug Code Directory, covering 11 finished drugs by generic name. By type: 24 prescription drugs. Its main marketing category is new drug applications (NDA). The newest product started marketing on July 1, 2026.
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- Labeler code
- 52427
- Products in commercial distribution
- 24
- Packages
- 24
- Finished drugs by generic name
- 11
- Prescription products
- 24
- Over the counter products
- 0
- Controlled substance products
- Schedule IV 5
- Flagged as original packager
- 11 of 11 products that carry the flag
- Started marketing in the last 12 months
- 3
- Products with a marketing end date set
- 2
- Earliest marketing start
- May 31, 2011
- openFDA record search
- api.fda.gov
Products by marketing category
Share of the company's products in commercial distribution.
| Marketing category | Products | Share |
|---|---|---|
| New drug applications (NDA) | 24 | 100% |
Products by type
| Type | Products | Share |
|---|---|---|
| Prescription drugs | 24 | 100% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Gabapentin | 5 | 91 |
| Lorazepam | 4 | 38 |
| Duloxetine | 3 | 36 |
| Lisinopril and hydrochlorothiazide | 3 | 21 |
| Sertraline hydrochloride | 2 | 55 |
| Naproxen sodium | 2 | 100 |
| Nitrofurantoin monohydrate/macrocrystalline | 1 | 4 |
| Venlafaxine | 1 | 33 |
| Escitalopram | 1 | 34 |
| Citalopram | 1 | 31 |
| Zolpidem tartrate | 1 | 38 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Capsule | 6 | 25% |
| Tablet, film coated | 5 | 20.8% |
| Capsule, extended release | 4 | 16.7% |
| Capsule, delayed release | 3 | 12.5% |
| Tablet | 3 | 12.5% |
| Tablet, film coated, extended release | 2 | 8.3% |
| Tablet, extended release | 1 | 4.2% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Duloxetine | 52427-913 | Capsule, delayed release | New drug applications (NDA) | July 1, 2026 |
| Duloxetine | 52427-821 | Capsule, delayed release | New drug applications (NDA) | July 1, 2026 |
| Duloxetine | 52427-791 | Capsule, delayed release | New drug applications (NDA) | July 1, 2026 |
| Escitalopram | 52427-795 | Capsule | New drug applications (NDA) | October 6, 2025 |
| Gralise | 52427-890 | Tablet, film coated | New drug applications (NDA) | December 31, 2023 |
| Gralise | 52427-850 | Tablet, film coated | New drug applications (NDA) | December 31, 2023 |
| Gralise | 52427-804 | Tablet, film coated | New drug applications (NDA) | December 31, 2023 |
| Zolpidem tartrate | 52427-775 | Capsule | New drug applications (NDA) | May 9, 2023 |
| Venlafaxine | 52427-632 | Tablet, extended release | New drug applications (NDA) | June 30, 2022 |
| Loreev xr | 52427-661 | Capsule, extended release | New drug applications (NDA) | March 1, 2022 |
| Citalopram | 52427-691 | Capsule | New drug applications (NDA) | January 31, 2022 |
| Sertraline HCl | 52427-672 | Capsule | New drug applications (NDA) | October 4, 2021 |
| Sertraline HCl | 52427-664 | Capsule | New drug applications (NDA) | October 4, 2021 |
| Loreev xr | 52427-667 | Capsule, extended release | New drug applications (NDA) | August 31, 2021 |
| Loreev xr | 52427-663 | Capsule, extended release | New drug applications (NDA) | August 31, 2021 |
| Loreev xr | 52427-658 | Capsule, extended release | New drug applications (NDA) | August 31, 2021 |
| Gralise | 52427-806 | Tablet, film coated | New drug applications (NDA) | October 1, 2020 |
| Gralise | 52427-803 | Tablet, film coated | New drug applications (NDA) | October 1, 2020 |
| Zestoretic | 52427-437 | Tablet | New drug applications (NDA) | April 15, 2015 |
| Zestoretic | 52427-436 | Tablet | New drug applications (NDA) | April 15, 2015 |
| Zestoretic | 52427-435 | Tablet | New drug applications (NDA) | April 15, 2015 |
| Naprelan | 52427-273 | Tablet, film coated, extended release | New drug applications (NDA) | January 17, 2014 |
| Naprelan | 52427-272 | Tablet, film coated, extended release | New drug applications (NDA) | January 17, 2014 |
| Macrobid | 52427-285 | Capsule | New drug applications (NDA) | May 31, 2011 |
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.