Ibuprofen

Product NDC
0615-2528
11-digit product format
006152528
Labeler code
0615
Product ID
0615-2528_c475ada9-5948-45e4-934f-571e46b9a38d
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Ibuprofen
Dosage form
TABLET
Route
ORAL
Labeler
NCS HealthCare of KY, Inc dba Vangard Labs
Application
ANDA078558
Marketing category
ANDA
Marketing start
2009-11-23
Marketing end
0000-00-00
Substance
IBUPROFEN
Active strength
800 mg/1
Pharmacologic classes
Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],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
0615-2528-392021-06-28C16284748780-19d75b9cf-d0dc-f424-e053-dadaa90a57ce10a13157-0c0b-4d54-9e49-7d78ed6fb9e8
0615-2528-392020-01-31C16284748780-19d75b9cf-d0dc-f424-e053-dadaa90a57ce10a13157-0c0b-4d54-9e49-7d78ed6fb9e8