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NDC
69339-123
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 NDC
Billing unit
Product NDC
DailyMed indexing SPL
SPL version
Effective
69339-123-06
EA - Each
69339-123
29e4279b-7f3c-4758-87fa-95583225ef3f
1
2016-05-16
Related Records
#
FDA application 200540
Company: Dash Pharmaceuticals LLC
Search ingredient/name matches
Related UNII Ingredients
#
UNII, Preferred term, Registry number table
UNII
Preferred term
Registry number
Matched term
QTG126297Q
DICLOFENAC SODIUM
15307-79-6
DICLOFENAC SODIUM
0E43V0BB57
MISOPROSTOL
59122-46-2
MISOPROSTOL