NDC codes

FDA NDC Directory
Product NDC (as listed)67046-0789Labeler and product segments. Claims need a package NDC.
Product NDC at billing width67046-0789Add 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
67046-0789-36704607890330 TABLET, DELAYED RELEASE in 1 BLISTER PACK (67046-0789-3)Marketed from Jun 19, 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)
Pantoprazole
Generic name (nonproprietary)
pantoprazole
Active ingredients
Pantoprazole sodium — 20 mg/1
Dosage form
Tablet, Delayed release
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 077619
Marketing start
Listing expires
Other FDA classes
Proton Pump Inhibitors (Mechanism)
Identifiers
Product ID 67046-0789_549da000-8699-22e2-e063-6394a90a8fccSPL ID 549da000-8699-22e2-e063-6394a90a8fccSPL set ID 549da3e8-f223-2ee7-e063-6394a90a25d8RxCUI 251872UNII 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

N467046078903 followed by a unit qualifier and the quantity

Package 67046-0789-03. 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 .

Indications (excerpt from the label)

Pantoprazole sodium delayed-release tablets are indicated for: Pantoprazole sodium is a proton pump inhibitor (PPI) indicated for the following: Short-Term Treatment of Erosive Esophagitis Associated with Gastroesophageal Reflux Disease (GERD) ( 1.1 ) Maintenance of Healing of Erosive Esophagitis ( 1.2 ) Pathological Hypersecretory Conditions Including Zollinger-Ellison (ZE) Syndrome ( 1.3 ) 1.1 Short-Term Treatment of Erosive Esophagitis Associated With Gastroesophageal Reflux Disease (GERD) Pantoprazole sodium delayed-release tablets are 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 …

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 077619

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

FDA NDC Directory listings under ANDA 077619
ProductStrengthForm · routeLabelerProduct NDC
PantoprazolePantoprazole sodium 20 mg/1Tablet, Delayed releaseOralSt. Mary's Medical Park Pharmacy60760-574
PantoprazolePantoprazole sodium 20 mg/1Tablet, Delayed releaseOralPreferred Pharmaceuticals Inc.68788-8505
PantoprazolePantoprazole sodium 20 mg/1Tablet, Delayed releaseOralPHOENIX RX LLC85509-1332
PantoprazolePantoprazole sodium 20 mg/1Tablet, Delayed releaseOralAdvanced Rx of Tennessee, LLC80425-0552
PantoprazolePantoprazole sodium 20 mg/1Tablet, Delayed releaseOralDr.Reddy's Laboratories Limited55111-332
PantoprazolePantoprazole sodium 40 mg/1Tablet, Delayed releaseOralDr.Reddy's Laboratories Limited55111-333
PantoprazolePantoprazole sodium 40 mg/1Tablet, Delayed releaseOralNuCare Pharmaceuticals,Inc.68071-3995
PantoprazolePantoprazole sodium 40 mg/1Tablet, Delayed releaseOralNuCare Pharmaceuticals,Inc.68071-3524
PantoprazolePantoprazole sodium 20 mg/1Tablet, Delayed releaseOralNuCare Pharmaceuticals, Inc.68071-3776
PantoprazolePantoprazole sodium 20 mg/1Tablet, Delayed releaseOralNorthStar RxLLC72603-177
PantoprazolePantoprazole sodium 40 mg/1Tablet, Delayed releaseOralNorthStar RxLLC72603-178

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