NDC 68788-8697 – Diclofenac Potassium

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

Human Prescription Drug

Product NDC68788-8697

Product details

Brand name
Diclofenac Potassium
Generic name
Diclofenac potassium
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA215585
Marketed since
June 24, 2024
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 (3)

Package NDCDescriptionSince
68788-8697-330 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-8697-3)Jun 24, 2024
68788-8697-660 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-8697-6)Jun 24, 2024
68788-8697-990 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-8697-9)Jun 24, 2024

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