Oxcarbazepine

Product NDC
0615-6594
11-digit product format
006156594
Labeler code
0615
Product ID
0615-6594_91255d9d-4ef6-474b-a073-286fa6e6e5e3
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Oxcarbazepine
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
NCS HealthCare of KY, Inc dba Vangard Labs
Application
ANDA077794
Marketing category
ANDA
Marketing start
2007-10-09
Marketing end
0000-00-00
Substance
OXCARBAZEPINE
Active strength
300 mg/1
Pharmacologic classes
Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [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
0615-6594-392021-07-29C16284748780-19d75b9d0-8677-f424-e053-dadaa90a57ceb28905b2-f99a-4b4a-9dc4-c0a06d7b0689
0615-6594-392020-01-31C16284748780-19d75b9d0-8677-f424-e053-dadaa90a57ceb28905b2-f99a-4b4a-9dc4-c0a06d7b0689