Etodolac NDC 71205-467

Product information

Brand name (proprietary)

Etodolac

Generic name (nonproprietary)

etodolac

Active ingredients

Etodolac — 500 mg/1

Dosage form

Tablet, Film coated

Route

Oral

Labeler

Proficient Rx LP

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 076004

Marketing start

May 1, 2003

Listing expires

Dec 31, 2026

Other FDA classes

Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)

Identifiers

Product ID 71205-467_5c5cba7e-33d5-4a93-ad61-ceff43cbd79eSPL ID 5c5cba7e-33d5-4a93-ad61-ceff43cbd79eSPL set ID 0c783997-6f2a-45ae-b899-c060c8be468aRxCUI 199390UNII 2M36281008UPC 0371205467609

Pharmacologic class

Nonsteroidal Anti-inflammatory Drug

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

N471205046730 followed by a unit qualifier and the quantity Copy

Package 71205-0467-30. 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 076004

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