Esomeprazole Magnesium NDC 73581-014

Product information

Brand name (proprietary)

Esomeprazole Magnesium

Generic name (nonproprietary)

esomeprazole magnesium

Active ingredients

Esomeprazole magnesium — 20 mg/1

Dosage form

Capsule

Route

Oral

Labeler

YYBA CORP

Product type

Over-the-counter drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 209339

Marketing start

Apr 1, 2026

Listing expires

Dec 31, 2027

Other FDA classes

Cytochrome P450 2C19 Inhibitors (Mechanism)Proton Pump Inhibitors (Mechanism)

Identifiers

Product ID 73581-014_4a7f3a55-8630-111f-e063-6294a90a6a44SPL ID 4a7f3a55-8630-111f-e063-6294a90a6a44SPL set ID 4a7f3a55-862f-111f-e063-6294a90a6a44RxCUI 606726UNII R6DXU4WAY9UPC 0373581000265

Pharmacologic class

Proton Pump Inhibitor

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N473581001442 followed by a unit qualifier and the quantity Copy

Package 73581-0014-42. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Other NDCs under ANDA 209339

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.