Diclofenac Sodium and Misoprostol

Product NDC
69339-123
11-digit product format
693390123
Labeler code
69339
Product ID
69339-123_4f699505-4205-4430-8959-8e929b986112
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Diclofenac Sodium and Misoprostol
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Labeler
Dash Pharmaceuticals LLC
Application
ANDA200540
Marketing category
ANDA
Marketing start
2015-02-18
Marketing end
2019-08-31
Substance
DICLOFENAC SODIUM; MISOPROSTOL
Active strength
50 mg/1; mg/1
Pharmacologic classes
Cyclooxygenase Inhibitors [MoA],Decreased Prostaglandin Production [PE],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC],Prostaglandin E1 Analog [EPC],Prostaglandins E, Synthetic [CS]
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
69339-123-06EA - Each69339-12329e4279b-7f3c-4758-87fa-95583225ef3f12016-05-16