NDC 71335-2441 – Diclofenac Sodium Misoprostol

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

Human Prescription Drug

Product NDC71335-2441

Product details

Brand name
Diclofenac Sodium Misoprostol
Generic name
Diclofenac sodium and misoprostol
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA205143
Marketed since
July 15, 2021
Listing expires
December 31, 2027
Pharmacologic class
Nonsteroidal Anti-inflammatory Drug; Prostaglandin E1 Analog

Active ingredients

Uses, dosage, side effects and warnings for Diclofenac Sodium/Misoprostol →

Package NDC codes (5)

Package NDCDescriptionSince
71335-2441-120 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2441-1)Sep 18, 2024
71335-2441-214 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2441-2)Sep 18, 2024
71335-2441-360 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2441-3)Sep 18, 2024
71335-2441-430 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2441-4)Sep 18, 2024
71335-2441-510 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2441-5)Sep 18, 2024

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