Esomeprazole Magnesium NDC 68071-3735

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

NuCare Pharmaceuticals,Inc.

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 078279

Marketing start

Sep 17, 2019

Listing expires

Dec 31, 2026

Other FDA classes

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

Identifiers

Product ID 68071-3735_33dd409c-d59c-d1e3-e063-6294a90a0ffbSPL ID 33dd409c-d59c-d1e3-e063-6294a90a0ffbSPL set ID 2879c79f-bf2a-0bc9-e063-6394a90a98aeRxCUI 606726UNII R6DXU4WAY9UPC 0368071373561

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

N468071373503 followed by a unit qualifier and the quantity Copy

Package 68071-3735-03. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 078279

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