NDC 71335-1183 – Diclofenac Sodium and Misoprostol

Diclofenac Sodium 75 mg/1; Misoprostol 200 ug/1 · Tablet, Delayed Release · Oral

Human Prescription Drug

Product NDC71335-1183

Product details

Brand name
Diclofenac Sodium and Misoprostol
Generic name
Diclofenac Sodium and Misoprostol
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA203995
Marketed since
December 1, 2016
Listing expires
December 31, 2026
Pharmacologic class
Nonsteroidal Anti-inflammatory Drug; Prostaglandin E1 Analog

Active ingredients

Uses, dosage, side effects and warnings for Diclofenac sodium and Misoprostol →

Package NDC codes (5)

Package NDCDescriptionSince
71335-1183-120 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1183-1)Jan 29, 2025
71335-1183-214 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1183-2)Apr 10, 2019
71335-1183-360 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1183-3)Jan 29, 2025
71335-1183-430 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1183-4)Jan 29, 2025
71335-1183-510 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1183-5)Jan 29, 2025

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