NDC 71335-9665 – Diclofenac sodium

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

Human Prescription Drug

Product NDC71335-9665

Product details

Brand name
Diclofenac sodium
Generic name
Diclofenac sodium
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA216275
Marketed since
September 26, 2022
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
71335-9665-0100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-9665-0)Apr 13, 2026
71335-9665-160 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-9665-1)Mar 22, 2023
71335-9665-230 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-9665-2)Mar 23, 2023
71335-9665-315 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-9665-3)Apr 13, 2026
71335-9665-414 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-9665-4)Mar 20, 2023
71335-9665-510 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-9665-5)Sep 24, 2024
71335-9665-621 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-9665-6)Jan 24, 2024
71335-9665-790 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-9665-7)Apr 13, 2026
71335-9665-8120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-9665-8)Apr 13, 2026
71335-9665-97 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-9665-9)Apr 13, 2026

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