NDC 71335-0456 – Diclofenac Sodium

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

Human Prescription Drug

Product NDC71335-0456

Product details

Brand name
Diclofenac Sodium
Generic name
Diclofenac Sodium
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA077863
Marketed since
August 19, 2008
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 (10)

Package NDCDescriptionSince
71335-0456-040 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0456-0)Aug 24, 2009
71335-0456-128 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0456-1)Aug 24, 2009
71335-0456-260 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0456-2)Aug 24, 2009
71335-0456-320 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0456-3)Aug 24, 2009
71335-0456-430 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0456-4)Aug 24, 2009
71335-0456-5120 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0456-5)Aug 24, 2009
71335-0456-690 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0456-6)Aug 24, 2009
71335-0456-7100 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0456-7)Aug 24, 2009
71335-0456-815 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0456-8)Aug 24, 2009
71335-0456-914 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0456-9)Aug 24, 2009

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