Esomeprazole magnesium NDC 21130-718

Product information

Brand name (proprietary)

Esomeprazole magnesium

Generic name (nonproprietary)

esomeprazole magnesium

Active ingredients

Esomeprazole magnesium — 20 mg/1

Dosage form

Capsule, Delayed release

Route

Oral

Labeler

BETTER LIVING BRANDS, LLC

Product type

Over-the-counter drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 217264

Marketing start

Oct 20, 2023

Listing expires

Dec 31, 2026

Other FDA classes

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

Identifiers

Product ID 21130-718_0a55d8b3-0539-2e0d-e063-6294a90a92a4SPL ID 0a55d8b3-0539-2e0d-e063-6294a90a92a4SPL set ID eb4c1cac-89a2-c040-e053-2995a90ae1cdRxCUI 606726UNII R6DXU4WAY9UPC 0321130277033

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

N421130071841 followed by a unit qualifier and the quantity Copy

Package 21130-0718-41. 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 217264

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