Omeprazole NDC 83209-150

Product information

Brand name (proprietary)

Omeprazole

Generic name (nonproprietary)

omeprazole

Active ingredients

Omeprazole — 20 mg/1

Dosage form

Capsule, Delayed release

Route

Oral

Labeler

Boswell Pharmacy Services LLC d/b/a BPS Wholesale

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 212977

Marketing start

Jun 12, 2024

Listing expires

Dec 31, 2026

Other FDA classes

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

Identifiers

Product ID 83209-150_1ab3d2c4-43c7-504d-e063-6394a90a9ba9SPL ID 1ab3d2c4-43c7-504d-e063-6394a90a9ba9SPL set ID 1ab3d84c-c563-6f04-e063-6394a90a34ffRxCUI 198051UNII 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

N483209015005 followed by a unit qualifier and the quantity Copy

Package 83209-0150-05. 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 212977

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