NDC 71335-0648 – Diclofenac Sodium

Diclofenac Sodium 100 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug

Product NDC71335-0648

Product details

Brand name
Diclofenac Sodium
Generic name
Diclofenac Sodium
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA075492
Marketed since
February 28, 2000
Listing expires
December 31, 2026
Pharmacologic class
Nonsteroidal Anti-inflammatory Drug

Active ingredients

Uses, dosage, side effects and warnings for Diclofenac Sodium →

Package NDC codes (9)

Package NDCDescriptionSince
71335-0648-160 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0648-1)May 22, 2018
71335-0648-230 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0648-2)Apr 13, 2018
71335-0648-315 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0648-3)Jan 29, 2025
71335-0648-414 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0648-4)Jul 23, 2018
71335-0648-510 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0648-5)Oct 13, 2022
71335-0648-621 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0648-6)Jul 3, 2018
71335-0648-790 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0648-7)Apr 16, 2019
71335-0648-8120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0648-8)Jan 29, 2025
71335-0648-97 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0648-9)Jan 29, 2025

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