What is NDC 68788-4060?

68788-4060 is the product NDC for Rabeprazole sodium, Rabeprazole sodium 20 mg/1 tablet, delayed release, listed with the FDA by Preferred Pharmaceuticals Inc.. It has 3 package NDCs, shown above in 10- and 11-digit form.

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 Rabeprazole sodium?

34 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Rabeprazole sodium NDC 68788-4060 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)68788-4060Labeler and product segments. Claims need a package NDC.

Product NDC at billing width68788-4060Add 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
68788-4060-3	6878840600368788406003	30 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-4060-3)Marketed from Dec 8, 2025
68788-4060-6	6878840600668788406006	60 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-4060-6)Marketed from Dec 8, 2025
68788-4060-9	6878840600968788406009	90 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-4060-9)Marketed from Dec 8, 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): Rabeprazole sodium
Generic name (nonproprietary): rabeprazole sodium
Active ingredients: Rabeprazole sodium — 20 mg/1
Dosage form: Tablet, Delayed release
Route: Oral
Labeler: Preferred Pharmaceuticals Inc.NDC labeler code 68788
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 202376
Marketing start: Dec 8, 2025
Listing expires: Dec 31, 2026
Other FDA classes: Proton Pump Inhibitors (Mechanism)
Identifiers: Product ID 68788-4060_1855ccab-c377-4962-9225-3c5adc62e2bdSPL ID 1855ccab-c377-4962-9225-3c5adc62e2bdSPL set ID 1855ccab-c377-4962-9225-3c5adc62e2bdRxCUI 854868UNII 3L36P16U4R
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

N468788406003 followed by a unit qualifier and the quantity

Package 68788-4060-03. 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 Dec 8, 2025.

Indications (excerpt from the label)

Rabeprazole sodium delayed-release tablets is a proton pump inhibitor (PPI) indicated in adults for: • Healing of Erosive or Ulcerative Gastroesophageal Reflux Disease (GERD) ( 1.1 ). • Maintenance of Healing of Erosive or Ulcerative GERD ( 1.2 ). • Treatment of Symptomatic GERD ( 1.3 ). • Healing of Duodenal Ulcers ( 1.4 ). • Helicobacter pylori Eradication to Reduce Risk of Duodenal Ulcer Recurrence ( 1.5 ). • Treatment of Pathological Hypersecretory Conditions, Including Zollinger-Ellison Syndrome ( 1.6 ). In adolescent patients 12 years of age and older for: • Short-term Treatment of Symptomatic GERD ( 1.7 ). 1.1 Healing of Erosive or Ulcerative GERD in Adults Rabeprazole sodium delayed-…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 68788-4060

What is NDC 68788-4060?: 68788-4060 is the product NDC for Rabeprazole sodium, Rabeprazole sodium 20 mg/1 tablet, delayed release, listed with the FDA by Preferred Pharmaceuticals Inc.. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Rabeprazole sodium.
What is the active ingredient?: Rabeprazole sodium.
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 Rabeprazole sodium?: 34 other product NDCs are listed under this name. See all Rabeprazole sodium 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 Rabeprazole sodium NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Rabeprazole Sodium	Rabeprazole sodium 20 mg/1	Tablet, Delayed releaseOral	Advanced Rx of Tennessee, LLC	80425-0449	80425-0449-0180425-0449-0280425-0449-03
Rabeprazole Sodium	Rabeprazole sodium 20 mg/1	Tablet, Delayed releaseOral	Advanced Rx of Tennessee, LLC	80425-0363	80425-0363-0180425-0363-0280425-0363-03
Rabeprazole Sodium	Rabeprazole sodium 20 mg/1	Tablet, Delayed releaseOral	Preferred Pharmaceuticals Inc.	68788-8536	68788-8536-0368788-8536-06
Rabeprazole Sodium	Rabeprazole sodium 20 mg/1	Tablet, Delayed releaseOral	REMEDYREPACK INC.	70518-3209	70518-3209-01
Rabeprazole Sodium	Rabeprazole sodium 20 mg/1	Tablet, Delayed releaseOral	St. Mary's Medical Park Pharmacy	60760-972	60760-0972-0760760-0972-30
Rabeprazole Sodium	Rabeprazole sodium 20 mg/1	Tablet, Delayed releaseOral	DIRECT RX	72189-169	72189-0169-3072189-0169-6072189-0169-90
Rabeprazole Sodium	Rabeprazole sodium 20 mg/1	Tablet, Delayed releaseOral	DIRECT RX	72189-142	72189-0142-3072189-0142-90
Rabeprazole Sodium	Rabeprazole sodium 20 mg/1	Tablet, Delayed releaseOral	REMEDYREPACK INC.	70518-2590	70518-2590-0070518-2590-01
Rabeprazole Sodium	Rabeprazole sodium 20 mg/1	Tablet, Delayed releaseOral	St. Mary's Medical Park Pharmacy	60760-560	60760-0560-0760760-0560-3060760-0560-60
Rabeprazole Sodium	Rabeprazole sodium 20 mg/1	Tablet, Delayed releaseOral	PHOENIX RX LLC	85509-1443	85509-1443-0385509-1443-0685509-1443-09

All 35 Rabeprazole sodium NDCs

Other NDCs under ANDA 202376

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

FDA NDC Directory listings under ANDA 202376
Product	Strength	Form · route	Labeler	Product NDC
Rabeprazole sodium	Rabeprazole sodium 20 mg/1	Tablet, Delayed releaseOral	Torrent Pharmaceuticals Limited	13668-107
Rabeprazole sodium	Rabeprazole sodium 20 mg/1	Tablet, Delayed releaseOral	Proficient Rx LP	63187-555