What is NDC 72189-514?

72189-514 is the product NDC for Pantoprazole Sodium DR, Pantoprazole sodium 40 mg/1 tablet, delayed release, listed with the FDA by Direct_Rx. It has 2 package NDCs, shown above in 10- and 11-digit form.

Direct_Rx, NDC labeler code 72189. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Pantoprazole Sodium DR?

6 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Pantoprazole Sodium DR NDC 72189-514

NDC codes

FDA NDC Directory

Product NDC (as listed)72189-514Labeler and product segments. Claims need a package NDC.

Product NDC at billing width72189-0514Add 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
72189-514-30	7218905143072189051430	30 TABLET, DELAYED RELEASE in 1 BOTTLE (72189-514-30)Marketed from Sep 11, 2023
72189-514-90	7218905149072189051490	90 TABLET, DELAYED RELEASE in 1 BOTTLE (72189-514-90)Marketed from Sep 11, 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): Pantoprazole Sodium DR
Generic name (nonproprietary): pantoprazole sodium dr
Active ingredients: Pantoprazole sodium — 40 mg/1
Dosage form: Tablet, Delayed release
Route: Oral
Labeler: Direct_RxNDC labeler code 72189
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 202882
Marketing start: Sep 11, 2023
Listing expires: Dec 31, 2027
Other FDA classes: Proton Pump Inhibitors (Mechanism)
Identifiers: Product ID 72189-514_4c4adb93-e6cf-6f33-e063-6294a90a063bSPL ID 4c4adb93-e6cf-6f33-e063-6294a90a063bSPL set ID 0515ceaa-7d17-c92f-e063-6294a90a044eRxCUI 314200UNII 6871619Q5X
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

N472189051430 followed by a unit qualifier and the quantity

Package 72189-0514-30. 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 Mar 5, 2026.

Indications (excerpt from the label)

Pantoprazole Sodium Delayed-Release Tablets are indicated for: 1.1 Short-Term Treatment of Erosive Esophagitis Associated With Gastroesophageal Reflux Disease (GERD) Pantoprazole Sodium Delayed-Release Tablet is indicated in adults and pediatric patients five years of age and older for the short-term treatment (up to 8 weeks) in the healing and symptomatic relief of erosive esophagitis (EE). For those adult patients who have not healed after 8 weeks of treatment, an additional 8-week course of pantoprazole sodium delayed-release tablets may be considered. Safety of treatment beyond 8 weeks in pediatric patients has not been established. 1.2 Maintenance of Healing of Erosive Esophagitis Panto…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 72189-514

What is NDC 72189-514?: 72189-514 is the product NDC for Pantoprazole Sodium DR, Pantoprazole sodium 40 mg/1 tablet, delayed release, listed with the FDA by Direct_Rx. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Pantoprazole Sodium DR.
What is the active ingredient?: Pantoprazole sodium.
Who is the labeler?: Direct_Rx, NDC labeler code 72189. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Pantoprazole Sodium DR?: 6 other product NDCs are listed under this name. See all Pantoprazole 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 Pantoprazole Sodium DR NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Pantoprazole Sodium DRpantoprazole sodium	Pantoprazole sodium 20 mg/1	Tablet, Delayed releaseOral	Advanced Rx of Tennessee, LLC	80425-0406	80425-0406-0180425-0406-0280425-0406-03
Pantoprazole Sodium DRpantoprazole sodium	Pantoprazole sodium 20 mg/1	Tablet, Delayed releaseOral	Advanced Rx Pharmacy of Tennessee, LLC	80425-0278	80425-0278-0180425-0278-0280425-0278-03
Pantoprazole Sodium DRpantoprazole sodium	Pantoprazole sodium 20 mg/1	Tablet, Delayed releaseOral	Advanced Rx of Tennessee, LLC	80425-0085	80425-0085-03
Pantoprazole Sodium DRpantoprazole sodium	Pantoprazole sodium 40 mg/1	Tablet, Delayed releaseOral	Advanced Rx Pharmacy of Tennessee, LLC	80425-0133	80425-0133-0180425-0133-0280425-0133-03
Pantoprazole Sodium DRpantoprazole sodium	Pantoprazole sodium 40 mg/1	Tablet, Delayed releaseOral	Advanced Rx Pharmacy of Tennessee, LLC	80425-0162	80425-0162-0180425-0162-0280425-0162-03
Pantoprazole Sodium DRpantoprazole sodium	Pantoprazole sodium 20 mg/1	Tablet, Delayed releaseOral	Advanced Rx Pharmacy of Tennessee, LLC	80425-0179	80425-0179-0280425-0179-03

Other NDCs under ANDA 202882

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

FDA NDC Directory listings under ANDA 202882
Product	Strength	Form · route	Labeler	Product NDC
Pantoprazole Sodiumpantoprazole	Pantoprazole sodium 20 mg/1	Tablet, Delayed releaseOral	Northwind Health Company, LLC	51655-744
Pantoprazole Sodium DRpantoprazole sodium	Pantoprazole sodium 20 mg/1	Tablet, Delayed releaseOral	Advanced Rx Pharmacy of Tennessee, LLC	80425-0278
Pantoprazole Sodiumpantoprazole	Pantoprazole sodium 40 mg/1	Tablet, Delayed releaseOral	AvPAK	50268-727
Pantoprazole Sodiumpantoprazole	Pantoprazole sodium 40 mg/1	Tablet, Delayed releaseOral	NuCare Pharmaceuticals,Inc.	68071-4864
Pantoprazole Sodiumpantoprazole	Pantoprazole sodium 20 mg/1	Tablet, Delayed releaseOral	Proficient Rx LP	63187-831
Pantoprazole Sodiumpantoprazole	Pantoprazole sodium 40 mg/1	Tablet, Delayed releaseOral	Bryant Ranch Prepack	71335-0551
Pantoprazole Sodiumpantoprazole	Pantoprazole sodium 40 mg/1	Tablet, Delayed releaseOral	A-S Medication Solutions	50090-5794
Pantoprazole Sodiumpantoprazole	Pantoprazole sodium 20 mg/1	Tablet, Delayed releaseOral	A-S Medication Solutions	50090-5793
Pantoprazole Sodiumpantoprazole	Pantoprazole sodium 20 mg/1	Tablet, Delayed releaseOral	Bryant Ranch Prepack	71335-1572
Pantoprazole Sodiumpantoprazole	Pantoprazole sodium 40 mg/1	Tablet, Delayed releaseOral	Aphena Pharma Solutions - Tennessee, LLC	71610-653
Pantoprazole Sodiumpantoprazole	Pantoprazole sodium 20 mg/1	Tablet, Delayed releaseOral	Aphena Pharma Solutions - Tennessee, LLC	71610-659
Pantoprazole Sodiumpantoprazole	Pantoprazole sodium 40 mg/1	Tablet, Delayed releaseOral	HAWAII REPACK, INC.	85534-0028
Pantoprazole Sodium DRpantoprazole sodium	Pantoprazole sodium 40 mg/1	Tablet, Delayed releaseOral	Advanced Rx Pharmacy of Tennessee, LLC	80425-0133
Pantoprazole Sodiumpantoprazole	Pantoprazole sodium 20 mg/1	Tablet, Delayed releaseOral	HAWAII REPACK, INC.	85534-0062
Pantoprazole Sodiumpantoprazole	Pantoprazole sodium 40 mg/1	Tablet, Delayed releaseOral	Proficient Rx LP	63187-654
Pantoprazole Sodiumpantoprazole	Pantoprazole sodium 40 mg/1	Tablet, Delayed releaseOral	St. Mary's Medical Park Pharmacy	60760-679
Pantoprazole Sodiumpantoprazole	Pantoprazole sodium 20 mg/1	Tablet, Delayed releaseOral	XLCare Pharmaceuticals Inc.	72865-229
Pantoprazole Sodiumpantoprazole	Pantoprazole sodium 40 mg/1	Tablet, Delayed releaseOral	XLCare Pharmaceuticals Inc.	72865-230
Pantoprazole Sodium DRpantoprazole sodium	Pantoprazole sodium 40 mg/1	Tablet, Delayed releaseOral	Advanced Rx Pharmacy of Tennessee, LLC	80425-0162
Pantoprazole Sodiumpantoprazole	Pantoprazole sodium 20 mg/1	Tablet, Delayed releaseOral	Quallent Pharmaceuticals Health LLC	82009-010

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