Diclofenac Sodium

Product NDC
51079-466
11-digit product format
510790466
Labeler code
51079
Product ID
51079-466_7be93f39-d61d-501e-e053-2991aa0a70be
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
diclofenac sodium
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Labeler
Mylan Institutional Inc.
Application
ANDA075281
Marketing category
ANDA
Marketing start
2010-06-04
Marketing end
0000-00-00
Substance
DICLOFENAC SODIUM
Active strength
50 mg/1
Pharmacologic classes
Cyclooxygenase Inhibitors [MoA],Decreased Prostaglandin Production [PE],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC]
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
51079-466-01EA - Each51079-4661f5bcdbf-20de-49ea-9e48-8c288c13010512012-07-24
51079-466-20EA - Each51079-466e499b11d-53c9-4c4d-ba97-f0b296aff5d112012-07-24