diclofenac sodium

Product NDC
0615-4506
11-digit product format
006154506
Labeler code
0615
Product ID
0615-4506_4d48eca9-541a-43b1-9345-23eeb66ca022
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
diclofenac sodium
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Labeler
NCS HealthCare of KY, Inc dba Vangard Labs
Application
ANDA074514
Marketing category
ANDA
Marketing start
1996-03-26
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
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0615-4506-392021-04-17C16284748780-19d75b9d0-5c3e-f424-e053-dadaa90a57ce70c96b78-3702-4216-819f-1071770494bf
0615-4506-392020-01-31C16284748780-19d75b9d0-5c3e-f424-e053-dadaa90a57ce70c96b78-3702-4216-819f-1071770494bf