Acid Reducer (omeprazole) NDC 63941-006

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

Best Choice

Product type

Over-the-counter drug

Marketing category

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

Marketing start

Jun 6, 2018

Listing expires

Dec 31, 2026

Other FDA classes

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

Identifiers

Product ID 63941-006_3a3a6029-3c1c-4c22-863d-1bf12733c39fSPL ID 3a3a6029-3c1c-4c22-863d-1bf12733c39fSPL set ID 43ea758b-6cea-44a2-b4d6-8f99211c8826RxCUI 402014UNII 426QFE7XLKUPC 0070038655015

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

N463941000605 followed by a unit qualifier and the quantity Copy

Package 63941-0006-05. 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.