NDC 63629-4108 – Diclofenac Potassium

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

Human Prescription Drug

Product NDC63629-4108

Product details

Brand name
Diclofenac Potassium
Generic name
Diclofenac Potassium
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA075219
Marketed since
August 11, 1998
Listing expires
December 31, 2026
Pharmacologic class
Nonsteroidal Anti-inflammatory Drug

Active ingredients

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

Package NDC codes (8)

Package NDCDescriptionSince
63629-4108-120 TABLET, FILM COATED in 1 BOTTLE (63629-4108-1)Dec 2, 2009
63629-4108-290 TABLET, FILM COATED in 1 BOTTLE (63629-4108-2)Apr 20, 2010
63629-4108-330 TABLET, FILM COATED in 1 BOTTLE (63629-4108-3)May 25, 2010
63629-4108-460 TABLET, FILM COATED in 1 BOTTLE (63629-4108-4)Jan 6, 2011
63629-4108-545 TABLET, FILM COATED in 1 BOTTLE (63629-4108-5)Dec 22, 2021
63629-4108-658 TABLET, FILM COATED in 1 BOTTLE (63629-4108-6)Dec 22, 2021
63629-4108-718 TABLET, FILM COATED in 1 BOTTLE (63629-4108-7)Dec 22, 2021
63629-4108-8120 TABLET, FILM COATED in 1 BOTTLE (63629-4108-8)Dec 22, 2021

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