Acid Reducer (esomeprazole magnesium) NDC 69842-679

NDC codes

FDA NDC Directory

Product NDC (as listed)69842-679Labeler and product segments. Claims need a package NDC.

Product NDC at billing width69842-0679Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
69842-679-14	69842067914	1 BOTTLE, PLASTIC in 1 CARTON (69842-679-14) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTICMarketed from Dec 31, 2021
69842-679-42	69842067942	3 BOTTLE, PLASTIC in 1 CARTON (69842-679-42) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTICMarketed from Dec 31, 2021

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Acid Reducer
Generic name (nonproprietary): esomeprazole magnesium
Active ingredients: Esomeprazole magnesium — 20 mg/1
Dosage form: Tablet, Delayed release
Route: Oral
Labeler: CVS Pharmacy
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 212088
Marketing start: Dec 31, 2021
Marketing end: Apr 30, 2027
Other FDA classes: Cytochrome P450 2C19 Inhibitors (Mechanism)Proton Pump Inhibitors (Mechanism)
Identifiers: Product ID 69842-679_5f0bc616-6126-4f48-b56c-e8874aed6e90SPL ID 5f0bc616-6126-4f48-b56c-e8874aed6e90SPL set ID 001817ea-906e-47f7-8605-41ba5a9abd21RxCUI 433733UNII R6DXU4WAY9
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

N469842067914 followed by a unit qualifier and the quantity

Package 69842-0679-14. 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

Current FDA label (SPL), effective Jan 21, 2026.

Indications (excerpt from the label)

Uses treats frequent heartburn (occurs 2 or more days a week) not intended for immediate relief of heartburn; this drug may take 1 to 4 days for full effect

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 212088

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

FDA NDC Directory listings under ANDA 212088
Product	Strength	Form · route	Labeler	Product NDC
Acid Reduceresomeprazole magnesium	Esomeprazole magnesium 20 mg/1	TabletOral	Walgreens	0363-9977