NDC 71335-9720 – Diclofenac Potassium

Diclofenac Potassium 50 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-9720

Product details

Brand name
Diclofenac Potassium
Generic name
Diclofenac Potassium Tablets
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA215750
Marketed since
May 12, 2022
Listing expires
December 31, 2027
Pharmacologic class
Nonsteroidal Anti-inflammatory Drug

Active ingredients

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

Package NDC codes (9)

Package NDCDescriptionSince
71335-9720-120 TABLET, FILM COATED in 1 BOTTLE (71335-9720-1)Apr 9, 2026
71335-9720-290 TABLET, FILM COATED in 1 BOTTLE (71335-9720-2)Oct 17, 2023
71335-9720-330 TABLET, FILM COATED in 1 BOTTLE (71335-9720-3)May 11, 2023
71335-9720-460 TABLET, FILM COATED in 1 BOTTLE (71335-9720-4)Nov 15, 2023
71335-9720-545 TABLET, FILM COATED in 1 BOTTLE (71335-9720-5)Apr 9, 2026
71335-9720-658 TABLET, FILM COATED in 1 BOTTLE (71335-9720-6)Apr 9, 2026
71335-9720-718 TABLET, FILM COATED in 1 BOTTLE (71335-9720-7)Apr 9, 2026
71335-9720-8120 TABLET, FILM COATED in 1 BOTTLE (71335-9720-8)Apr 9, 2026
71335-9720-9100 TABLET, FILM COATED in 1 BOTTLE (71335-9720-9)Apr 9, 2026

Other Diclofenac Potassium products