NDC 71335-1958 – Etodolac

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

Human Prescription Drug

Product NDC71335-1958

Product details

Brand name
Etodolac
Generic name
Etodolac
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA075074
Marketed since
March 11, 1998
Listing expires
December 31, 2027
Pharmacologic class
Nonsteroidal Anti-inflammatory Drug

Active ingredients

Uses, dosage, side effects and warnings for Etodolac →

Package NDC codes (8)

Package NDCDescriptionSince
71335-1958-120 TABLET, FILM COATED in 1 BOTTLE (71335-1958-1)Aug 20, 2026
71335-1958-214 TABLET, FILM COATED in 1 BOTTLE (71335-1958-2)Aug 20, 2026
71335-1958-330 TABLET, FILM COATED in 1 BOTTLE (71335-1958-3)Dec 7, 2021
71335-1958-4100 TABLET, FILM COATED in 1 BOTTLE (71335-1958-4)Aug 20, 2026
71335-1958-560 TABLET, FILM COATED in 1 BOTTLE (71335-1958-5)Sep 27, 2021
71335-1958-690 TABLET, FILM COATED in 1 BOTTLE (71335-1958-6)Oct 18, 2021
71335-1958-756 TABLET, FILM COATED in 1 BOTTLE (71335-1958-7)Oct 11, 2021
71335-1958-8120 TABLET, FILM COATED in 1 BOTTLE (71335-1958-8)Aug 20, 2026

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