NDC 71335-2052 – Diclofenac Potassium

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

Human Prescription Drug

Product NDC71335-2052

Product details

Brand name
Diclofenac Potassium
Generic name
Diclofenac potassium
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA075229
Marketed since
December 19, 2020
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
71335-2052-120 TABLET, COATED in 1 BOTTLE (71335-2052-1)Mar 18, 2022
71335-2052-290 TABLET, COATED in 1 BOTTLE (71335-2052-2)Mar 18, 2022
71335-2052-330 TABLET, COATED in 1 BOTTLE (71335-2052-3)Mar 16, 2022
71335-2052-460 TABLET, COATED in 1 BOTTLE (71335-2052-4)Feb 16, 2022
71335-2052-545 TABLET, COATED in 1 BOTTLE (71335-2052-5)Mar 18, 2022
71335-2052-658 TABLET, COATED in 1 BOTTLE (71335-2052-6)Mar 18, 2022
71335-2052-718 TABLET, COATED in 1 BOTTLE (71335-2052-7)Mar 18, 2022
71335-2052-8120 TABLET, COATED in 1 BOTTLE (71335-2052-8)Mar 18, 2022
71335-2052-9100 TABLET, COATED in 1 BOTTLE (71335-2052-9)Mar 18, 2022

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