Omeprazole NDC 62756-377

Product information

Brand name (proprietary)

Omeprazole

Generic name (nonproprietary)

omeprazole

Active ingredients

Omeprazole — 20 mg/1

Dosage form

Tablet, Delayed release

Route

Oral

Labeler

Sun Pharmaceutical Industries, Inc.

Product type

Over-the-counter drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 207891

Marketing start

Jan 1, 2019

Listing expires

Dec 31, 2026

Other FDA classes

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

Identifiers

Product ID 62756-377_676e2f39-d83e-485a-9366-ed14c382e466SPL ID 676e2f39-d83e-485a-9366-ed14c382e466SPL set ID 51c3ef34-b7c1-419e-a784-ae82540c7a22RxCUI 402014UNII KG60484QX9

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

N462756037711 followed by a unit qualifier and the quantity Copy

Package 62756-0377-11. 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 207891

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