NDC 51655-735 – Etodolac

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

Human Prescription Drug

Product NDC51655-735

Product details

Brand name
Etodolac
Generic name
Etodolac
Labeler
Northwind Health Company, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA208834
Marketed since
July 8, 2021
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
51655-735-5230 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-735-52)Jul 8, 2021

Other Etodolac products