NDC 71335-2684 – Diclofenac Sodium

Diclofenac Sodium 75 mg/1 · Tablet, Delayed Release · Oral

Human Prescription Drug

Product NDC71335-2684

Product details

Brand name
Diclofenac Sodium
Generic name
Diclofenac Sodium
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA216548
Marketed since
May 11, 2023
Listing expires
December 31, 2027
Pharmacologic class
Nonsteroidal Anti-inflammatory Drug

Active ingredients

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

Package NDC codes (10)

Package NDCDescriptionSince
71335-2684-040 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2684-0)Feb 13, 2026
71335-2684-128 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2684-1)Feb 13, 2026
71335-2684-260 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2684-2)Feb 13, 2026
71335-2684-320 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2684-3)Feb 13, 2026
71335-2684-430 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2684-4)Feb 13, 2026
71335-2684-5120 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2684-5)Feb 13, 2026
71335-2684-690 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2684-6)Feb 13, 2026
71335-2684-7100 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2684-7)Feb 13, 2026
71335-2684-815 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2684-8)Feb 13, 2026
71335-2684-914 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2684-9)Feb 13, 2026

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