Drug company (FDA labeler)
Almatica Pharma LLC
NDC labeler code: 52427
What is a labeler?
The company whose name is on the package and in the FDA’s National Drug Code (NDC) Directory. It may make the medicine itself or sell medicine made by another company. The first part of every NDC code identifies the labeler.
Official FDA data only
Products, approvals and recalls come from the FDA (NDC Directory, Drugs@FDA, enforcement reports). Recalls are linked to this company by the NDC labeler code on the recalled product.
Questions about your medicine: ask your doctor or pharmacist. In an emergency, call 911.
Prescription medicines
- GabapentinNeurontin, Gralise, Relgaabi · 5 products
- LorazepamAtivan, Loreev XR · 4 products
- DuloxetineDrizalma Sprinkle · 3 products
- NaproxenNaprelan, Rugby All Day Relief · 2 products
- Sertraline hydrochlorideZoloft · 2 products
- Nitrofurantoin (monohydrate/macrocrystals)Macrobid, Nitrofurantoin Monohydrate Macrocrystalline, Nitrofurantoin Mono · 1 product
- Venlafaxine1 product
- CitalopramCelexa · 1 product
- EscitalopramLexapro · 1 product
- Zolpidem tartrateAmbien, Ambien CR, Edluar · 1 product
FDA applications for these products
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
| Approved | Application | Medicine | Sponsor |
|---|---|---|---|
| February 27, 2026 | NDA219131 | Duloxetine DULOXETINE HYDROCHLORIDE | Almatica |
| August 29, 2025 | NDA219130 | Escitalopram ESCITALOPRAM | Almatica |
| May 9, 2023 | NDA215721 | Zolpidem tartrate ZOLPIDEM TARTRATE | Almatica |
| June 29, 2022 | NDA215429 | Venlafaxine VENLAFAXINE BESYLATE | Almatica |
| January 31, 2022 | NDA215428 | Citalopram CITALOPRAM HYDROBROMIDE | Almatica |
| October 4, 2021 | NDA215133 | Sertraline hydrochloride SERTRALINE HYDROCHLORIDE | Almatica |
| August 27, 2021 | NDA214826 | Lorazepam LOREEV XR | Almatica |
| January 28, 2011 | NDA022544 | Gabapentin GRALISE | Almatica |
| January 5, 1996 | NDA020353 | Naproxen NAPRELAN | Twi Pharms |
| December 24, 1991 | NDA020064 | Nitrofurantoin (monohydrate/macrocrystals) MACROBID | Almatica |
The sponsor is the company that holds the FDA application; it can differ from the labeler.
Recall timeline
No recall of these products (by NDC code) appears in the FDA enforcement reports.
Next steps
- Find a pharmacy near youAsk which company made your medicine and whether it is recalled
- Latest FDA drug recallsAll companies, newest first
- All drug companiesA to Z
- All prescription drugs A to ZSearch by generic, brand or Spanish name
Sources
- NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026