NDC 80425-0381 – Etodolac

Etodolac 600 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug

Product NDC80425-0381

Product details

Brand name
Etodolac
Generic name
Etodolac
Labeler
Advanced Rx Pharmacy of Tennessee, LLC
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA091134
Marketed since
April 10, 2024
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
80425-0381-130 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (80425-0381-1)Apr 10, 2024

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