NDC codes

FDA NDC Directory
Product NDC (as listed)0615-7629Labeler and product segments. Claims need a package NDC.
Product NDC at billing width00615-7629Add 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
0615-7629-05006157629050061576290515 TABLET, DELAYED RELEASE in 1 BLISTER PACK (0615-7629-05)Marketed from Apr 6, 2022
0615-7629-0700615762907006157629077 TABLET, DELAYED RELEASE in 1 BLISTER PACK (0615-7629-07)Marketed from Apr 6, 2022
0615-7629-14006157629140061576291414 TABLET, DELAYED RELEASE in 1 BLISTER PACK (0615-7629-14)Marketed from Apr 6, 2022
0615-7629-28006157629280061576292828 TABLET, DELAYED RELEASE in 1 BLISTER PACK (0615-7629-28)Marketed from Apr 24, 2024
0615-7629-3000615762930006157629306 BLISTER PACK in 1 BOX, UNIT-DOSE (0615-7629-30) / 5 TABLET, DELAYED RELEASE in 1 BLISTER PACKMarketed from Apr 11, 2022
0615-7629-39006157629390061576293930 TABLET, DELAYED RELEASE in 1 BLISTER PACK (0615-7629-39)Marketed from Apr 6, 2022

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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
Generic name (nonproprietary)
pantoprazole sodium
Active ingredients
Pantoprazole sodium — 40 mg/1
Dosage form
Tablet, Delayed release
Route
Oral
Labeler
NCS HealthCare of KY, LLC dba Vangard LabsNDC labeler code 0615
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 090970
Marketing start
Marketing end
Other FDA classes
Proton Pump Inhibitors (Mechanism)
Identifiers
Product ID 0615-7629_11b463e4-96eb-4169-bf13-aa55ab7838e5SPL ID 11b463e4-96eb-4169-bf13-aa55ab7838e5
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

N400615762905 followed by a unit qualifier and the quantity

Package 00615-7629-05. 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

The FDA listing for this product does not reference a label (SPL) set.

About NDC 0615-7629

What is NDC 0615-7629?
0615-7629 is the product NDC for Pantoprazole Sodium, Pantoprazole sodium 40 mg/1 tablet, delayed release, listed with the FDA by NCS HealthCare of KY, LLC dba Vangard Labs. It has 6 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Pantoprazole Sodium.
What is the active ingredient?
Pantoprazole sodium.
Who is the labeler?
NCS HealthCare of KY, LLC dba Vangard Labs, NDC labeler code 0615. 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?
135 other product NDCs are listed under this name. See all Pantoprazole 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 Pantoprazole Sodium NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Pantoprazole SodiumPantoprazole sodium 40 mg/10mLInjection, Powder, Lyophilized, For solutionIntravenousAvenacy, LLC83634-75183634-0751-10
Pantoprazole SodiumPantoprazole sodium 40 mg/1Tablet, Delayed releaseOralCardinal Health 107, LLC55154-028955154-0289-00
Pantoprazole SodiumpantoprazolePantoprazole sodium 40 mg/1Tablet, Delayed releaseOralAvPAK50268-72750268-0727-10
Pantoprazole SodiumPantoprazole sodium 40 mg/1Tablet, Delayed releaseOralUnit Dose Solutions, Inc.87441-06687441-0066-01
Pantoprazole SodiumPantoprazole sodium 20 mg/1Tablet, Delayed releaseOralUnit Dose Solutions, Inc.87441-06587441-0065-01
Pantoprazole SodiumPantoprazole sodium 20 mg/1Tablet, Delayed releaseOralCoupler LLC67046-034767046-0347-03
Pantoprazole SodiumPantoprazole sodium 40 mg/1Tablet, Delayed releaseOralCoupler LLC67046-053667046-0536-03
Pantoprazole SodiumPantoprazole sodium 40 mg/1Tablet, Delayed releaseOralSafecor Health LLC48433-08148433-0081-20
Pantoprazole SodiumPantoprazole sodium 40 mg/1Tablet, Delayed releaseOralNorthStar Rx LLC72603-74672603-0746-0172603-0746-02
Pantoprazole SodiumPantoprazole sodium 40 mg/10mLInjection, Powder, For solutionIntravenousDevatis Inc.73043-02073043-0020-0173043-0020-1073043-0020-25

All 136 Pantoprazole Sodium NDCs

Other NDCs under ANDA 090970

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

FDA NDC Directory listings under ANDA 090970
ProductStrengthForm · routeLabelerProduct NDC
Pantoprazole SodiumPantoprazole sodium 20 mg/1Tablet, Delayed releaseOralMylan Pharmaceuticals Inc.0378-6688
Pantoprazole SodiumPantoprazole sodium 40 mg/1Tablet, Delayed releaseOralMylan Pharmaceuticals Inc.0378-6689
Pantoprazole SodiumPantoprazole sodium 40 mg/1Tablet, Delayed releaseOralQPharma Inc42708-180
Pantoprazole SodiumPantoprazole sodium 40 mg/1Tablet, Delayed releaseOralSafecor Health LLC48433-081
Pantoprazole SodiumPantoprazole sodium 40 mg/1Tablet, Delayed releaseOralMylan Institutional Inc.51079-051
Pantoprazole SodiumPantoprazole sodium 40 mg/1Tablet, Delayed releaseOralCardinal Health 107, LLC55154-0289
Pantoprazole SodiumPantoprazole sodium 40 mg/1Tablet, Delayed releaseOralCardinal Health 107, LLC55154-4382
Pantoprazole SodiumPantoprazole sodium 40 mg/1Tablet, Delayed releaseOralBryant Ranch Prepack71335-1429
Pantoprazole Sodium DRpantoprazole sodiumPantoprazole sodium 20 mg/1Tablet, Delayed releaseOralAdvanced Rx Pharmacy of Tennessee, LLC80425-0179

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