NDC 71335-2259 – Etodolac

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

Human Prescription Drug

Product NDC71335-2259

Product details

Brand name
Etodolac
Generic name
Etodolac
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA210704
Marketed since
August 1, 2021
Listing expires
December 31, 2026
Pharmacologic class
Nonsteroidal Anti-inflammatory Drug

Active ingredients

Uses, dosage, side effects and warnings for Etodolac →

Package NDC codes (8)

Package NDCDescriptionSince
71335-2259-120 TABLET, FILM COATED in 1 BOTTLE (71335-2259-1)Oct 30, 2023
71335-2259-214 TABLET, FILM COATED in 1 BOTTLE (71335-2259-2)Oct 30, 2023
71335-2259-330 TABLET, FILM COATED in 1 BOTTLE (71335-2259-3)Oct 30, 2023
71335-2259-4100 TABLET, FILM COATED in 1 BOTTLE (71335-2259-4)Oct 30, 2023
71335-2259-560 TABLET, FILM COATED in 1 BOTTLE (71335-2259-5)Oct 30, 2023
71335-2259-690 TABLET, FILM COATED in 1 BOTTLE (71335-2259-6)Oct 30, 2023
71335-2259-756 TABLET, FILM COATED in 1 BOTTLE (71335-2259-7)Oct 30, 2023
71335-2259-8120 TABLET, FILM COATED in 1 BOTTLE (71335-2259-8)Oct 30, 2023

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