Esomeprazole Magnesium NDC 75907-119

NDC codes

FDA NDC Directory

Product NDC (as listed)75907-119Labeler and product segments. Claims need a package NDC.

Product NDC at billing width75907-0119Add 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
75907-119-27	75907011927	2 BOTTLE in 1 CARTON (75907-119-27) / 14 TABLET, DELAYED RELEASE in 1 BOTTLEMarketed from Dec 30, 2023
75907-119-33	75907011933	3 BOTTLE in 1 CARTON (75907-119-33) / 14 TABLET, DELAYED RELEASE in 1 BOTTLEMarketed from Dec 30, 2023
75907-119-52	75907011952	1 BOTTLE in 1 CARTON (75907-119-52) / 14 TABLET, DELAYED RELEASE in 1 BOTTLEMarketed from Dec 30, 2023

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): Esomeprazole Magnesium
Generic name (nonproprietary): esomeprazole magnesium
Active ingredients: Esomeprazole magnesium — 20 mg/1
Dosage form: Tablet, Delayed release
Route: Oral
Labeler: Dr. Reddys Laboratories Inc
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 211571
Marketing start: Dec 30, 2023
Listing expires: Dec 31, 2026
Other FDA classes: Cytochrome P450 2C19 Inhibitors (Mechanism)Proton Pump Inhibitors (Mechanism)
Identifiers: Product ID 75907-119_a40c48e8-93c4-8b65-6b4d-a6d236e39c38SPL ID a40c48e8-93c4-8b65-6b4d-a6d236e39c38SPL set ID 2c2bcdf7-689a-47bd-1713-0ea74f72044bRxCUI 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

N475907011927 followed by a unit qualifier and the quantity

Package 75907-0119-27. 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 Dec 14, 2023.

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 211571

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

FDA NDC Directory listings under ANDA 211571
Product	Strength	Form · route	Labeler	Product NDC
Esomeprazole Magnesium	Esomeprazole magnesium 20 mg/1	Tablet, Delayed releaseOral	Walgreens	0363-1353
Esomeprazole Magnesium	Esomeprazole magnesium 20 mg/1	Tablet, Delayed releaseOral	Dr. Reddys Laboratories Inc	43598-069
Esomeprazole Magnesium	Esomeprazole magnesium 20 mg/1	Tablet, Delayed releaseOral	CVS Pharmacy	51316-563