Pantoprazole NDC 55111-332

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

Dr.Reddy's Laboratories Limited

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 077619

Marketing start

Jan 19, 2011

Listing expires

Dec 31, 2027

Other FDA classes

Proton Pump Inhibitors (Mechanism)

Identifiers

Product ID 55111-332_c0575fc6-20c4-12a6-10b7-1af65cac1ee0SPL ID c0575fc6-20c4-12a6-10b7-1af65cac1ee0SPL set ID 564709e8-358f-c185-4ecb-b3849c3fe59cRxCUI 251872, 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

N455111033201 followed by a unit qualifier and the quantity Copy

Package 55111-0332-01. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 077619

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