NDC 71335-2530 – Diclofenac Potassium

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

Human Prescription Drug

Product NDC71335-2530

Product details

Brand name
Diclofenac Potassium
Generic name
Diclofenac potassium
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA215585
Marketed since
October 11, 2021
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
71335-2530-120 TABLET, FILM COATED in 1 BOTTLE (71335-2530-1)Nov 25, 2024
71335-2530-290 TABLET, FILM COATED in 1 BOTTLE (71335-2530-2)Nov 25, 2024
71335-2530-330 TABLET, FILM COATED in 1 BOTTLE (71335-2530-3)Nov 25, 2024
71335-2530-460 TABLET, FILM COATED in 1 BOTTLE (71335-2530-4)Nov 25, 2024
71335-2530-545 TABLET, FILM COATED in 1 BOTTLE (71335-2530-5)Nov 25, 2024
71335-2530-658 TABLET, FILM COATED in 1 BOTTLE (71335-2530-6)Nov 25, 2024
71335-2530-718 TABLET, FILM COATED in 1 BOTTLE (71335-2530-7)Nov 25, 2024
71335-2530-8120 TABLET, FILM COATED in 1 BOTTLE (71335-2530-8)Nov 25, 2024
71335-2530-9100 TABLET, FILM COATED in 1 BOTTLE (71335-2530-9)Nov 25, 2024

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