What is NDC 72657-124?

72657-124 is the product NDC for esomeprazole magnesium, Esomeprazole magnesium 20 mg/1 capsule, delayed release, listed with the FDA by GLENMARK THERAPEUTICS INC., USA. It has 1 package NDC, shown above in 10- and 11-digit form.

GLENMARK THERAPEUTICS INC., USA, NDC labeler code 72657. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for esomeprazole magnesium?

179 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

esomeprazole magnesium NDC 72657-124

NDC codes

FDA NDC Directory

Product NDC (as listed)72657-124Labeler and product segments. Claims need a package NDC.

Product NDC at billing width72657-0124Add 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
72657-124-42	7265701244272657012442	3 BOTTLE in 1 CARTON (72657-124-42) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLEMarketed from Aug 22, 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: Capsule, Delayed release
Route: Oral
Labeler: GLENMARK THERAPEUTICS INC., USANDC labeler code 72657
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 216349
Marketing start: Aug 22, 2023
Listing expires: Dec 31, 2026
Other FDA classes: Cytochrome P450 2C19 Inhibitors (Mechanism)Proton Pump Inhibitors (Mechanism)
Identifiers: Product ID 72657-124_4744704a-027c-4925-9d57-99b4434fc946SPL ID 4744704a-027c-4925-9d57-99b4434fc946SPL set ID ff233fbb-716d-4879-811c-c8d82e3c99ceRxCUI 606726UNII R6DXU4WAY9UPC 0372657124423
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

N472657012442 followed by a unit qualifier and the quantity

Package 72657-0124-42. 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

Current FDA label (SPL), effective May 25, 2023.

Full label on DailyMed (opens in a new tab)

About NDC 72657-124

What is NDC 72657-124?: 72657-124 is the product NDC for esomeprazole magnesium, Esomeprazole magnesium 20 mg/1 capsule, delayed release, listed with the FDA by GLENMARK THERAPEUTICS INC., USA. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: esomeprazole magnesium.
What is the active ingredient?: Esomeprazole magnesium.
Who is the labeler?: GLENMARK THERAPEUTICS INC., USA, NDC labeler code 72657. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for esomeprazole magnesium?: 179 other product NDCs are listed under this name. See all esomeprazole magnesium NDCs.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other esomeprazole magnesium NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Esomeprazole Magnesium	Esomeprazole magnesium 20 mg/1	Capsule, Delayed releaseOral	REMEDYREPACK INC.	70518-4776	70518-4776-00
Esomeprazole Magnesium	Esomeprazole magnesium dihydrate 20 mg/1	Capsule, Delayed releaseOral	Chain Drug Marketing Association, Inc.	83324-328	83324-0328-1483324-0328-42
Esomeprazole Magnesium	Esomeprazole magnesium 20 mg/1	Capsule, Delayed releaseOral	St. Mary's Medical Park Pharmacy	60760-877	60760-0877-60
Esomeprazole Magnesiumesomeprazole	Esomeprazole 20 mg/1	Capsule, Delayed releaseOral	Amazon.com Services LLC	72288-563	72288-0563-01
esomeprazole magnesiumesomeprazole magnesium dihydrate	Esomeprazole magnesium dihydrate 20 mg/1	Capsule, Delayed releaseOral	Amazon.com Services LLC	72288-780	72288-0780-03
Esomeprazole Magnesium	Esomeprazole magnesium 20 mg/1	Capsule, Delayed releaseOral	American Health Packaging	60687-934	60687-0934-21
esomeprazole magnesiumesomeprazole	Esomeprazole 20 mg/1	Capsule, Delayed releaseOral	Amazon.com Services LLC	72288-669	72288-0669-0172288-0669-03
Esomeprazole Magnesium	Esomeprazole magnesium 20 mg/1	Capsule, Delayed releaseOral	H-E-B	37808-646	37808-0646-4137808-0646-4537808-0646-82
Esomeprazole Magnesium	Esomeprazole magnesium 20 mg/1	Capsule, Delayed releaseOral	Rising Pharma Holdings, Inc.	64980-664	64980-0664-1964980-0664-41
Esomeprazole Magnesium	Esomeprazole magnesium 20 mg/1	CapsuleOral	YYBA CORP	73581-014	73581-0014-42

All 180 esomeprazole magnesium NDCs

Other NDCs under ANDA 216349

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

FDA NDC Directory listings under ANDA 216349
Product	Strength	Form · route	Labeler	Product NDC
Esomeprazole Magnesium	Esomeprazole magnesium 20 mg/1	Capsule, Delayed releaseOral	Rising Pharma Holdings, Inc.	16571-880
Esomeprazole Magnesium	Esomeprazole magnesium 20 mg/1	Capsule, Delayed releaseOral	Rising Pharma Holdings, Inc.	64980-664
Esomeprazole Magnesium	Esomeprazole magnesium 20 mg/1	Capsule, Delayed releaseOral	Reliable 1 Laboratories LLC	69618-073
esomeprazole magnesium	Esomeprazole magnesium trihydrate 20 mg/1	Capsule, Delayed releaseOral	GLENMARK THERAPEUTICS INC., USA	72657-127