Pentoxifylline

Product NDC
0615-4523
11-digit product format
006154523
Labeler code
0615
Product ID
0615-4523_e71a3614-e3ae-4979-b6d9-1556c2ca2161
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Pentoxifylline
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Labeler
NCS HealthCare of KY, Inc dba Vangard Labs
Application
ANDA074425
Marketing category
ANDA
Marketing start
2009-09-21
Marketing end
0000-00-00
Substance
PENTOXIFYLLINE
Active strength
400 mg/1
Pharmacologic classes
Blood Viscosity Reducer [EPC],Hematologic Activity Alteration [PE]
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
0615-4523-392021-07-30C16284748780-19d75b9d0-4d5c-f424-e053-dadaa90a57ce7096593b-0054-4d51-83df-0208ccdcc147
0615-4523-392020-01-31C16284748780-19d75b9d0-4d5c-f424-e053-dadaa90a57ce7096593b-0054-4d51-83df-0208ccdcc147