Drug company (FDA labeler)
Wilshire Pharmaceuticals, Inc.
NDC labeler code: 52536
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
- Verapamil hydrochloride7 products
- DextroamphetamineZenzedi, Xelstrym, Dexedrine Spansule · 5 products
- Perphenazine4 products
- LomustineGleostine · 3 products
- Azilsartan kamedoxomilAzilsartan Medoxomil, Edarbi · 2 products
- CarisoprodolSoma · 2 products
- Sodium sulfate, potassium sulfate, magnesium sulfateSuprep Bowel Prep, Sodium Sulfate, Potassium Sulfate, and Magnesium Sulfate Bowel Prep Kit · 2 products
- AmphetamineAdzenys Xr-Odt, Dyanavel XR, Evekeo · 2 products
- DexmedetomidinePrecedex, Dexmedetomidine in Dextrose, Igalmi · 2 products
- Erythromycin ethylsuccinateEry-Ped, E.E.S 400, E.E.S · 2 products
- Polyethylene glycol 3350, sodium chloride, sodium bicarbonate, potassium chloridePEG 3350, Sodium Chloride, Sodium Bicarbonate and Potassium Chloride, Trilyte, Peg-3350, Sodium Chloride, Sodium Bicarbonate and Potassium Chloride · 1 product
- BaclofenGablofen, Lyvispah, Baclofen (Intrathecal) · 1 product
- Enalapril maleateVasotec, Epaned · 1 product
- Polyethylene glycol 3350, sodium sulfate anhydrous, sodium bicarbonate, sodium chloride, potassium chloridePeg-3350 and Electrolytes, Golytely, PEG 3350 and Electrolytes · 1 product
FDA applications for these products
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
- ANDA: Abbreviated New Drug Application: how a generic version is approved.
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.
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