NDC 68071-3731 – Etodolac

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

Human Prescription Drug

Product NDC68071-3731

Product details

Brand name
Etodolac
Generic name
Etodolac
Labeler
NuCare Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA091134
Marketed since
February 15, 2014
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
68071-3731-414 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68071-3731-4)Nov 27, 2024

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