NDC 0093-1118 – Etodolac

Etodolac 600 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug

Product NDC0093-1118

Product details

Brand name
Etodolac
Generic name
Etodolac
Labeler
Teva Pharmaceuticals USA, Inc.
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA075665
Marketed since
August 17, 2000
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
0093-1118-01100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0093-1118-01)Aug 17, 2000

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