Omeprazole NDC 71205-613

Product information

Brand name (proprietary)

Omeprazole

Generic name (nonproprietary)

omeprazole

Active ingredients

Omeprazole — 20 mg/1

Dosage form

Capsule, Delayed release

Route

Oral

Labeler

Proficient Rx LP

Product type

Prescription drug

Marketing category

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

Marketing start

Feb 20, 2019

Listing expires

Dec 31, 2026

Other FDA classes

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

Identifiers

Product ID 71205-613_d870bdc1-5e26-4153-89e2-f629fef60ad0SPL ID d870bdc1-5e26-4153-89e2-f629fef60ad0SPL set ID 13b379ef-7982-434d-9e6b-e01cd2b398d2RxCUI 198051UNII KG60484QX9UPC 0371205613303

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

N471205061306 followed by a unit qualifier and the quantity Copy

Package 71205-0613-06. 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 212977

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