NDC 71205-865 – Diclofenac Sodium Misoprostol

Diclofenac Sodium 50 mg/1; Misoprostol 200 ug/1 · Tablet, Delayed Release · Oral

Human Prescription Drug

Product NDC71205-865

Product details

Brand name
Diclofenac Sodium Misoprostol
Generic name
Diclofenac Sodium and Misoprostol
Labeler
Proficient Rx LP
Dosage form
Tablet, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA205143
Marketed since
July 15, 2021
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/Misoprostol →

Package NDC codes (7)

Package NDCDescriptionSince
71205-865-00100 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-865-00)Mar 7, 2022
71205-865-3030 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-865-30)Mar 7, 2022
71205-865-55500 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-865-55)Mar 7, 2022
71205-865-6060 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-865-60)Mar 7, 2022
71205-865-64240 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-865-64)Mar 7, 2022
71205-865-72120 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-865-72)Mar 7, 2022
71205-865-9090 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-865-90)Mar 7, 2022

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