Diclofenac Sodium

Product NDC
63629-5096
11-digit product format
636295096
Labeler code
63629
Product ID
63629-5096_9c87ec42-2bb0-491c-9499-4451c67cc55d
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Diclofenac Sodium
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
NDA020254
Marketing category
NDA AUTHORIZED GENERIC
Marketing start
1996-03-08
Marketing end
0000-00-00
Substance
DICLOFENAC SODIUM
Active strength
100 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
2021-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
63629-5096-16362950960130 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-5096-1) 2013-09-230000-00-00NoNoCurrent
63629-5096-26362950960260 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-5096-2) 2013-09-230000-00-00NoNoCurrent
63629-5096-36362950960390 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-5096-3) 2013-09-230000-00-00NoNoCurrent
63629-5096-463629509604120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-5096-4) 2013-09-230000-00-00NoNoCurrent