Tramadol Hydrochloride

Product NDC
0615-7810
11-digit product format
006157810
Labeler code
0615
Product ID
0615-7810_b33f3503-1b4c-4fbb-8b63-04971b39b554
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
tramadol hydrochloride
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
NCS HealthCare of KY, Inc dba Vangard Labs
Application
ANDA075986
Marketing category
ANDA
Marketing start
2002-06-21
Marketing end
0000-00-00
Substance
TRAMADOL HYDROCHLORIDE
Active strength
50 mg/1
Pharmacologic classes
Full Opioid Agonists [MoA],Opioid Agonist [EPC]
DEA schedule
CIV
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
0615-7810-392022-09-30C16284748780-19d75b9d0-c92b-f424-e053-dadaa90a57cef6d34d61-9175-4106-a497-0598b25212fa
0615-7810-392020-01-31C16284748780-19d75b9d0-c92b-f424-e053-dadaa90a57cef6d34d61-9175-4106-a497-0598b25212fa