NDC 80425-0551 – Etodolac

Etodolac 400 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC80425-0551

Product details

Brand name
Etodolac
Generic name
Etodolac
Labeler
Advanced Rx of Tennessee, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA075074
Marketed since
August 29, 2025
Listing expires
December 31, 2026
Pharmacologic class
Nonsteroidal Anti-inflammatory Drug

Active ingredients

Uses, dosage, side effects and warnings for Etodolac →

Package NDC codes (1)

Package NDCDescriptionSince
80425-0551-160 TABLET, FILM COATED in 1 BOTTLE (80425-0551-1)Aug 29, 2025

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