Diclofenac Sodium Misoprostol

Product NDC
71205-865
11-digit product format
712050865
Labeler code
71205
Product ID
71205-865_47a851b9-3e7f-4271-a2b8-ce836579729b
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Diclofenac Sodium and Misoprostol
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Labeler
Proficient Rx LP
Application
ANDA205143
Marketing category
ANDA
Marketing start
2021-07-15
Substance
DICLOFENAC SODIUM; MISOPROSTOL
Active strength
50; 200 mg/1; ug/1
Pharmacologic classes
Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Decreased Prostaglandin Production [PE], Nonsteroidal Anti-inflammatory Drug [EPC], Prostaglandin E1 Analog [EPC], Prostaglandins E, Synthetic [CS]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
QTG126297QDICLOFENAC SODIUM15307-79-6DICLOFENAC SODIUM
0E43V0BB57MISOPROSTOL59122-46-2MISOPROSTOL

Packages

Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
71205-865-0071205086500100 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-865-00) 2022-03-07NoNoHistorical
71205-865-307120508653030 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-865-30) 2022-03-07NoNoHistorical
71205-865-5571205086555500 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-865-55) 2022-03-07NoNoHistorical
71205-865-607120508656060 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-865-60) 2022-03-07NoNoHistorical
71205-865-6471205086564240 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-865-64) 2022-03-07NoNoHistorical
71205-865-7271205086572120 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-865-72) 2022-03-07NoNoHistorical
71205-865-907120508659090 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-865-90) 2022-03-07NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Diclofenac Sodium MisoprostolProficient Rx LP2022-07-01HUMAN PRESCRIPTION DRUG LABEL3