NDC 51655-423 – Etodolac

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

Human Prescription Drug

Product NDC51655-423

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
August 17, 2020
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
51655-423-5230 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-423-52)Aug 17, 2020

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