NDC 43063-856 – Etodolac

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

Human Prescription Drug

Product NDC43063-856

Product details

Brand name
Etodolac
Generic name
Etodolac
Labeler
PD-Rx Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076004
Marketed since
May 1, 2003
Listing expires
December 31, 2027
Pharmacologic class
Nonsteroidal Anti-inflammatory Drug

Active ingredients

Uses, dosage, side effects and warnings for Etodolac →

Package NDC codes (3)

Package NDCDescriptionSince
43063-856-2020 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-856-20)May 31, 2018
43063-856-3030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-856-30)Jun 27, 2018
43063-856-6060 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-856-60)Nov 1, 2018

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