NDC codes

FDA NDC Directory
Product NDC (as listed)80425-0134Labeler and product segments. Claims need a package NDC.
Product NDC at billing width80425-0134Add 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 NDC11-digit (billing)PackageCopy
80425-0134-1804250134018042501340130 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0134-1)Marketed from Apr 27, 2018
80425-0134-2804250134028042501340260 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0134-2)Marketed from Apr 27, 2018
80425-0134-3804250134038042501340390 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0134-3)Marketed from Apr 28, 2023
80425-0134-480425013404804250134046 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0134-4)Marketed from Mar 26, 2026

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 DRSuffix: DR
Generic name (nonproprietary)
rabeprazole sodium
Active ingredients
Rabeprazole sodium — 20 mg/1
Dosage form
Tablet, Delayed release
Route
Oral
Labeler
Advanced Rx Pharmacy of Tennessee, LLCNDC labeler code 80425
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 208644
Marketing start
Listing expires
Other FDA classes
Proton Pump Inhibitors (Mechanism)
Identifiers
Product ID 80425-0134_4df0b57a-090c-2350-e063-6394a90addbeSPL ID 4df0b57a-090c-2350-e063-6394a90addbeSPL set ID bdad0b58-495e-2352-e053-2a95a90a3198RxCUI 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

N480425013401 followed by a unit qualifier and the quantity

Package 80425-0134-01. 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 .

Indications (excerpt from the label)

1. Indications and Usage Section 1 INDICATIONS & USAGE 1.1 Healing of Erosive or Ulcerative GERD in Adults Rabeprazole sodium delayed-release tablets are indicated for short-term (4 to 8 weeks) treatment in the healing and symptomatic relief of erosive or ulcerative gastroesophageal reflux disease (GERD). For those patients who have not healed after 8 weeks of treatment, an additional 8-week course of rabeprazole sodium delayed-release tablets may be considered. 1.2 Maintenance of Healing of Erosive or Ulcerative GERD in Adults Rabeprazole sodium delayed-release tablets are indicated for maintaining healing and reduction in relapse rates of heartburn symptoms in patients with erosive or ulce…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 80425-0134

What is NDC 80425-0134?
80425-0134 is the product NDC for Rabeprazole Sodium DR (rabeprazole sodium), Rabeprazole sodium 20 mg/1 tablet, delayed release, listed with the FDA by Advanced Rx Pharmacy of Tennessee, LLC. It has 4 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Rabeprazole Sodium DR (Rabeprazole Sodium).
What is the active ingredient?
Rabeprazole sodium.
Who is the labeler?
Advanced Rx Pharmacy of Tennessee, LLC, NDC labeler code 80425. 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 DR?
1 other product NDC are listed under this name. See all Rabeprazole Sodium DR 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 DR NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Rabeprazole Sodium DRrabeprazole sodiumRabeprazole sodium 20 mg/1Tablet, Delayed releaseOralAdvanced Rx of Tennessee, LLC80425-009480425-0094-0180425-0094-0280425-0094-03

Other NDCs under ANDA 208644

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

FDA NDC Directory listings under ANDA 208644
ProductStrengthForm · routeLabelerProduct NDC
Rabeprazole SodiumRabeprazole sodium 20 mg/1Tablet, Delayed releaseOralA-S Medication Solutions50090-4751
Rabeprazole SodiumRabeprazole sodium 20 mg/1Tablet, Delayed releaseOralSt. Mary's Medical Park Pharmacy60760-560
Rabeprazole SodiumRabeprazole sodium 20 mg/1Tablet, Delayed releaseOralAscend Laboratories, LLC67877-443
Rabeprazole SodiumRabeprazole sodium 20 mg/1Tablet, Delayed releaseOralPreferred Pharmaceuticals, Inc.68788-7459
Rabeprazole SodiumRabeprazole sodium 20 mg/1Tablet, Delayed releaseOralREMEDYREPACK INC.70518-2590
Rabeprazole SodiumRabeprazole sodium 20 mg/1Tablet, Delayed releaseOralProficient Rx LP71205-292
Rabeprazole SodiumRabeprazole sodium 20 mg/1Tablet, Delayed releaseOralBryant Ranch Prepack71335-1100
Rabeprazole SodiumRabeprazole sodium 20 mg/1Tablet, Delayed releaseOralBryant Ranch Prepack72162-2367
Rabeprazole SodiumRabeprazole sodium 20 mg/1Tablet, Delayed releaseOralDIRECT RX72189-169
Rabeprazole SodiumRabeprazole sodium 20 mg/1Tablet, Delayed releaseOralAsclemed USA, Inc.76420-818
Rabeprazole SodiumRabeprazole sodium 20 mg/1Tablet, Delayed releaseOralPHOENIX RX LLC85509-1443
Rabeprazole Sodium DRrabeprazole sodiumRabeprazole sodium 20 mg/1Tablet, Delayed releaseOralAdvanced Rx of Tennessee, LLC80425-0094

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