NDC 68788-7315 – Etodolac

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

Human Prescription Drug

Product NDC68788-7315

Product details

Brand name
Etodolac
Generic name
Etodolac
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA208834
Marketed since
January 2, 2019
Listing expires
December 31, 2027
Pharmacologic class
Nonsteroidal Anti-inflammatory Drug

Active ingredients

Uses, dosage, side effects and warnings for Etodolac →

Package NDC codes (5)

Package NDCDescriptionSince
68788-7315-1100 TABLET, FILM COATED in 1 BOTTLE (68788-7315-1)Jan 2, 2019
68788-7315-220 TABLET, FILM COATED in 1 BOTTLE (68788-7315-2)Jan 2, 2019
68788-7315-330 TABLET, FILM COATED in 1 BOTTLE (68788-7315-3)Jan 2, 2019
68788-7315-660 TABLET, FILM COATED in 1 BOTTLE (68788-7315-6)Jan 2, 2019
68788-7315-990 TABLET, FILM COATED in 1 BOTTLE (68788-7315-9)Jan 2, 2019

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