NDC 71610-859 – Etodolac

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

Human Prescription Drug

Product NDC71610-859

Product details

Brand name
Etodolac
Generic name
Etodolac
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA075074
Marketed since
March 11, 1998
Listing expires
December 31, 2026
Pharmacologic class
Nonsteroidal Anti-inflammatory Drug

Active ingredients

Uses, dosage, side effects and warnings for Etodolac →

Package NDC codes (4)

Package NDCDescriptionSince
71610-859-3030 TABLET, FILM COATED in 1 BOTTLE (71610-859-30)Oct 10, 2024
71610-859-5360 TABLET, FILM COATED in 1 BOTTLE (71610-859-53)Oct 10, 2024
71610-859-6090 TABLET, FILM COATED in 1 BOTTLE (71610-859-60)Oct 10, 2024
71610-859-80180 TABLET, FILM COATED in 1 BOTTLE (71610-859-80)Oct 10, 2024

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