NDC 65841-779 – Etodolac

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

Human Prescription Drug

Product NDC65841-779

Product details

Brand name
Etodolac
Generic name
Etodolac
Labeler
Zydus Lifesciences Limited
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA091134
Marketed since
February 15, 2014
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
65841-779-01100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65841-779-01)Feb 15, 2014
65841-779-05500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65841-779-05)Feb 15, 2014
65841-779-101000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65841-779-10)Feb 15, 2014
65841-779-1460 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65841-779-14)Feb 15, 2014
65841-779-77100 BLISTER PACK in 1 CARTON (65841-779-77) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (65841-779-30)Feb 15, 2014

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