What is NDC 68788-8906?

68788-8906 is the product NDC for Naproxen and esomeprazole magnesium, Naproxen 375 mg/1; Esomeprazole magnesium trihydrate 20 mg/1 tablet, delayed release, listed with the FDA by Preferred Pharmaceuticals Inc. It has 2 package NDCs, shown above in 10- and 11-digit form.

What is the active ingredient?

Naproxen, Esomeprazole magnesium trihydrate.

Preferred Pharmaceuticals Inc, NDC labeler code 68788. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Naproxen and esomeprazole magnesium?

20 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Naproxen and esomeprazole magnesium NDC 68788-8906

NDC codes

FDA NDC Directory

Product NDC (as listed)68788-8906Labeler and product segments. Claims need a package NDC.

Product NDC at billing width68788-8906Add 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
68788-8906-3	6878889060368788890603	30 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-8906-3)Marketed from Jul 31, 2025
68788-8906-6	6878889060668788890606	60 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-8906-6)Marketed from Jul 31, 2025

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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): Naproxen and esomeprazole magnesium
Generic name (nonproprietary): naproxen and esomeprazole magnesium
Active ingredients: Naproxen — 375 mg/1Esomeprazole magnesium trihydrate — 20 mg/1
Dosage form: Tablet, Delayed release
Route: Oral
Labeler: Preferred Pharmaceuticals IncNDC labeler code 68788
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 217738
Marketing start: Jul 31, 2025
Listing expires: Dec 31, 2026
Other FDA classes: Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)Cytochrome P450 2C19 Inhibitors (Mechanism)Proton Pump Inhibitors (Mechanism)
Identifiers: Product ID 68788-8906_470496f5-a71d-40b2-bf11-3a8d3d790962SPL ID 470496f5-a71d-40b2-bf11-3a8d3d790962SPL set ID 470496f5-a71d-40b2-bf11-3a8d3d790962RxCUI 994005UNII 57Y76R9ATQ, R6DXU4WAY9
Pharmacologic class: Nonsteroidal Anti-inflammatory Drug; 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

N468788890603 followed by a unit qualifier and the quantity

Package 68788-8906-03. 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

Current FDA label (SPL), effective Jul 31, 2025. This label includes a boxed warning.

Indications (excerpt from the label)

Naproxen and esomeprazole magnesium delayed-release tablets, a combination of naproxen and esomeprazole magnesium, is indicated in adult and adolescent patients 12 years of age and older weighing at least 38 kg, requiring naproxen for symptomatic relief of arthritis and esomeprazole magnesium to decrease the risk for developing naproxen-associated gastric ulcers. The naproxen component of naproxen and esomeprazole magnesium delayed-release tablets are indicated for relief of signs and symptoms of: • osteoarthritis, rheumatoid arthritis and ankylosing spondylitis in adults. • juvenile idiopathic arthritis (JIA) in adolescent patients. The esomeprazole magnesium component of naproxen and esome…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 68788-8906

What is NDC 68788-8906?: 68788-8906 is the product NDC for Naproxen and esomeprazole magnesium, Naproxen 375 mg/1; Esomeprazole magnesium trihydrate 20 mg/1 tablet, delayed release, listed with the FDA by Preferred Pharmaceuticals Inc. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Naproxen and esomeprazole magnesium.
What is the active ingredient?: Naproxen, Esomeprazole magnesium trihydrate.
Who is the labeler?: Preferred Pharmaceuticals Inc, NDC labeler code 68788. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Naproxen and esomeprazole magnesium?: 20 other product NDCs are listed under this name. See all Naproxen and 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 Naproxen and esomeprazole magnesium NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Naproxen and esomeprazole magnesium	Naproxen 375 mg/1; Esomeprazole magnesium trihydrate 20 mg/1	Tablet, Delayed releaseOral	Preferred Pharmaceuticals Inc.	68788-4166	68788-4166-0368788-4166-06
Naproxen and esomeprazole magnesium	Naproxen 500 mg/1; Esomeprazole magnesium trihydrate 20 mg/1	Tablet, Delayed releaseOral	Preferred Pharmaceuticals Inc.	68788-4043	68788-4043-0368788-4043-06
Naproxen and esomeprazole magnesium	Naproxen 500 mg/1; Esomeprazole magnesium trihydrate 20 mg/1	Tablet, Delayed releaseOral	Preferred Pharmaceuticals Inc.	68788-8766	68788-8766-0368788-8766-06
Naproxen and esomeprazole magnesium	Naproxen 375 mg/1; Esomeprazole magnesium 20 mg/1	Tablet, Delayed releaseOral	ScieGen Pharmaceuticals, Inc	50228-437	50228-0437-1050228-0437-3050228-0437-60
Naproxen and esomeprazole magnesium	Naproxen 500 mg/1; Esomeprazole magnesium 20 mg/1	Tablet, Delayed releaseOral	ScieGen Pharmaceuticals, Inc	50228-438	50228-0438-0550228-0438-3050228-0438-60
Naproxen and esomeprazole magnesium	Naproxen 500 mg/1; Esomeprazole magnesium 20 mg/1	Tablet, Delayed releaseOral	Bryant Ranch Prepack	71335-2552	71335-2552-0171335-2552-02
Naproxen and esomeprazole magnesium	Naproxen 500 mg/1; Esomeprazole magnesium trihydrate 20 mg/1	Tablet, Delayed releaseOral	Proficient Rx LP	82804-303	82804-0303-60
Naproxen and esomeprazole magnesium	Naproxen 500 mg/1; Esomeprazole magnesium 20 mg/1	Tablet, Delayed releaseOral	PHOENIX RX LLC	85509-1438	85509-1438-0185509-1438-0385509-1438-06+1 more
Naproxen and esomeprazole magnesium	Naproxen 375 mg/1; Esomeprazole magnesium 20 mg/1	Tablet, Delayed releaseOral	Ajanta Pharma USA Inc.	27241-202	27241-0202-60
Naproxen and esomeprazole magnesium	Naproxen 500 mg/1; Esomeprazole magnesium 20 mg/1	Tablet, Delayed releaseOral	Ajanta Pharma USA Inc.	27241-203	27241-0203-60

All 21 Naproxen and esomeprazole magnesium NDCs

Other NDCs under ANDA 217738

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

FDA NDC Directory listings under ANDA 217738
Product	Strength	Form · route	Labeler	Product NDC
Naproxen and esomeprazole magnesium	Naproxen 375 mg/1; Esomeprazole magnesium 20 mg/1	Tablet, Delayed releaseOral	ScieGen Pharmaceuticals, Inc	50228-437
Naproxen and esomeprazole magnesium	Naproxen 500 mg/1; Esomeprazole magnesium 20 mg/1	Tablet, Delayed releaseOral	ScieGen Pharmaceuticals, Inc	50228-438
Naproxen and esomeprazole magnesium	Naproxen 500 mg/1; Esomeprazole magnesium 20 mg/1	Tablet, Delayed releaseOral	Bryant Ranch Prepack	71335-2552
Naproxen and esomeprazole magnesium	Naproxen 500 mg/1; Esomeprazole magnesium trihydrate 20 mg/1	Tablet, Delayed releaseOral	Proficient Rx LP	82804-303
Naproxen and esomeprazole magnesium	Naproxen 500 mg/1; Esomeprazole magnesium 20 mg/1	Tablet, Delayed releaseOral	PHOENIX RX LLC	85509-1438