Venlafaxine

Product NDC
0615-6567
11-digit product format
006156567
Labeler code
0615
Product ID
0615-6567_4cf939f3-8eda-42c2-84f4-45405768fa97
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Venlafaxine
Dosage form
TABLET
Route
ORAL
Labeler
NCS HealthCare of KY, Inc dba Vangard Labs
Application
ANDA077653
Marketing category
ANDA
Marketing start
2008-06-13
Marketing end
0000-00-00
Substance
VENLAFAXINE HYDROCHLORIDE
Active strength
75 mg/1
Pharmacologic classes
Norepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
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
0615-6567-392022-09-27C16284748780-19d75b9d1-2529-f424-e053-dadaa90a57ce2c7742aa-7722-4c12-9e4b-b4c3ca5a7fb0
0615-6567-392020-01-31C16284748780-19d75b9d1-2529-f424-e053-dadaa90a57ce2c7742aa-7722-4c12-9e4b-b4c3ca5a7fb0