NDC 51672-4018 – Etodolac

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

Human Prescription Drug

Product NDC51672-4018

Product details

Brand name
Etodolac
Generic name
Etodolac
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA075074
Marketed since
March 11, 1998
Listing expires
December 31, 2027
Pharmacologic class
Nonsteroidal Anti-inflammatory Drug

Active ingredients

Uses, dosage, side effects and warnings for Etodolac →

Package NDC codes (1)

Package NDCDescriptionSince
51672-4018-1100 TABLET, FILM COATED in 1 BOTTLE (51672-4018-1)Mar 11, 1998

Other Etodolac products