NDC 69238-1343 – Etodolac

Etodolac 500 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC69238-1343

Product details

Brand name
Etodolac
Generic name
Etodolac
Labeler
Amneal Pharmaceuticals NY LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA208834
Marketed since
June 11, 2018
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
69238-1343-1100 TABLET, FILM COATED in 1 BOTTLE (69238-1343-1)Jun 11, 2018

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