NDC 68788-8846 – Etodolac

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

Human Prescription Drug

Product NDC68788-8846

Product details

Brand name
Etodolac
Generic name
Etodolac
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076004
Marketed since
March 24, 2025
Listing expires
December 31, 2026
Pharmacologic class
Nonsteroidal Anti-inflammatory Drug

Active ingredients

Uses, dosage, side effects and warnings for Etodolac →

Package NDC codes (5)

Package NDCDescriptionSince
68788-8846-1100 TABLET, FILM COATED in 1 BOTTLE (68788-8846-1)Mar 24, 2025
68788-8846-220 TABLET, FILM COATED in 1 BOTTLE (68788-8846-2)Mar 24, 2025
68788-8846-330 TABLET, FILM COATED in 1 BOTTLE (68788-8846-3)Mar 24, 2025
68788-8846-660 TABLET, FILM COATED in 1 BOTTLE (68788-8846-6)Mar 24, 2025
68788-8846-990 TABLET, FILM COATED in 1 BOTTLE (68788-8846-9)Mar 24, 2025

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