Acid Reducer (omeprazole) NDC 55319-037

Product information

Brand name (proprietary)

Acid Reducer

Generic name (nonproprietary)

omeprazole

Active ingredients

Omeprazole magnesium — 20 mg/1

Dosage form

Tablet, Delayed release

Route

Oral

Labeler

Family Dollar Stores, LLC

Product type

Over-the-counter drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 206877

Marketing start

Jun 17, 2024

Listing expires

Dec 31, 2026

Other FDA classes

Cytochrome P450 2C19 Inhibitors (Mechanism)Proton Pump Inhibitors (Mechanism)

Identifiers

Product ID 55319-037_c1eee169-a04a-485d-9c17-2229cdca1fd1SPL ID c1eee169-a04a-485d-9c17-2229cdca1fd1SPL set ID 6d8daf78-1672-4bbf-a022-514bf0a5ac9aRxCUI 402014UNII 426QFE7XLK

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

N455319003705 followed by a unit qualifier and the quantity Copy

Package 55319-0037-05. 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

Other NDCs under ANDA 206877

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