What is NDC 85509-1332?

85509-1332 is the product NDC for Pantoprazole, Pantoprazole sodium 20 mg/1 tablet, delayed release, listed with the FDA by PHOENIX RX LLC. It has 3 package NDCs, shown above in 10- and 11-digit form.

PHOENIX RX LLC, NDC labeler code 85509. 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?

11 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Pantoprazole NDC 85509-1332 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)85509-1332Labeler and product segments. Claims need a package NDC.

Product NDC at billing width85509-1332Add 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
85509-1332-3	8550913320385509133203	30 TABLET, DELAYED RELEASE in 1 BOTTLE (85509-1332-3)Marketed from Nov 20, 2025
85509-1332-6	8550913320685509133206	60 TABLET, DELAYED RELEASE in 1 BOTTLE (85509-1332-6)Marketed from Nov 20, 2025
85509-1332-9	8550913320985509133209	90 TABLET, DELAYED RELEASE in 1 BOTTLE (85509-1332-9)Marketed from Nov 20, 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): Pantoprazole
Generic name (nonproprietary): pantoprazole
Active ingredients: Pantoprazole sodium — 20 mg/1
Dosage form: Tablet, Delayed release
Route: Oral
Labeler: PHOENIX RX LLCNDC labeler code 85509
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 077619
Marketing start: Jan 19, 2011
Listing expires: Dec 31, 2026
Other FDA classes: Proton Pump Inhibitors (Mechanism)
Identifiers: Product ID 85509-1332_43fc6335-4b31-60bc-e063-6294a90a7362SPL ID 43fc6335-4b31-60bc-e063-6294a90a7362SPL set ID 43fc6326-cfe6-7d1c-e063-6394a90abc24RxCUI 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

N485509133203 followed by a unit qualifier and the quantity

Package 85509-1332-03. 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 Nov 19, 2025.

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)

About NDC 85509-1332

What is NDC 85509-1332?: 85509-1332 is the product NDC for Pantoprazole, Pantoprazole sodium 20 mg/1 tablet, delayed release, listed with the FDA by PHOENIX RX LLC. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Pantoprazole.
What is the active ingredient?: Pantoprazole sodium.
Who is the labeler?: PHOENIX RX LLC, NDC labeler code 85509. 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?: 11 other product NDCs are listed under this name. See all Pantoprazole 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 NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Pantoprazole	Pantoprazole sodium 20 mg/1	Tablet, Delayed releaseOral	Coupler LLC	67046-0789	67046-0789-03
Pantoprazole	Pantoprazole sodium 20 mg/1	Tablet, Delayed releaseOral	Advanced Rx of Tennessee, LLC	80425-0552	80425-0552-0180425-0552-0280425-0552-03
Pantoprazole	Pantoprazole sodium 20 mg/1	Tablet, Delayed releaseOral	NuCare Pharmaceuticals, Inc.	68071-3776	68071-3776-0368071-3776-06
Pantoprazole	Pantoprazole sodium 40 mg/1	Tablet, Delayed releaseOral	NuCare Pharmaceuticals,Inc.	68071-3995	68071-3995-09
Pantoprazole	Pantoprazole sodium 20 mg/1	Tablet, Delayed releaseOral	NorthStar RxLLC	72603-177	72603-0177-01
Pantoprazole	Pantoprazole sodium 40 mg/1	Tablet, Delayed releaseOral	NorthStar RxLLC	72603-178	72603-0178-01
Pantoprazole	Pantoprazole sodium 20 mg/1	Tablet, Delayed releaseOral	Preferred Pharmaceuticals Inc.	68788-8505	68788-8505-0168788-8505-0368788-8505-06+2 more
Pantoprazole	Pantoprazole sodium 20 mg/1	Tablet, Delayed releaseOral	St. Mary's Medical Park Pharmacy	60760-574	60760-0574-3060760-0574-60
Pantoprazole	Pantoprazole sodium 20 mg/1	Tablet, Delayed releaseOral	Dr.Reddy's Laboratories Limited	55111-332	55111-0332-0155111-0332-0555111-0332-10+4 more
Pantoprazole	Pantoprazole sodium 40 mg/1	Tablet, Delayed releaseOral	Dr.Reddy's Laboratories Limited	55111-333	55111-0333-0155111-0333-0555111-0333-10+4 more

All 12 Pantoprazole NDCs

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
Product	Strength	Form · route	Labeler	Product NDC
Pantoprazole	Pantoprazole sodium 20 mg/1	Tablet, Delayed releaseOral	Coupler LLC	67046-0789
Pantoprazole	Pantoprazole sodium 20 mg/1	Tablet, Delayed releaseOral	Dr.Reddy's Laboratories Limited	55111-332
Pantoprazole	Pantoprazole sodium 40 mg/1	Tablet, Delayed releaseOral	Dr.Reddy's Laboratories Limited	55111-333
Pantoprazole	Pantoprazole sodium 40 mg/1	Tablet, Delayed releaseOral	NuCare Pharmaceuticals,Inc.	68071-3995
Pantoprazole	Pantoprazole sodium 20 mg/1	Tablet, Delayed releaseOral	Advanced Rx of Tennessee, LLC	80425-0552
Pantoprazole	Pantoprazole sodium 40 mg/1	Tablet, Delayed releaseOral	NuCare Pharmaceuticals,Inc.	68071-3524
Pantoprazole	Pantoprazole sodium 20 mg/1	Tablet, Delayed releaseOral	NuCare Pharmaceuticals, Inc.	68071-3776
Pantoprazole	Pantoprazole sodium 20 mg/1	Tablet, Delayed releaseOral	St. Mary's Medical Park Pharmacy	60760-574
Pantoprazole	Pantoprazole sodium 40 mg/1	Tablet, Delayed releaseOral	Redpharm Drug	67296-2355
Pantoprazole	Pantoprazole sodium 20 mg/1	Tablet, Delayed releaseOral	Preferred Pharmaceuticals Inc.	68788-8505
Pantoprazole	Pantoprazole sodium 40 mg/1	Tablet, Delayed releaseOral	NorthStar RxLLC	72603-178
Pantoprazole	Pantoprazole sodium 20 mg/1	Tablet, Delayed releaseOral	NorthStar RxLLC	72603-177