Terazosin

Product NDC
0615-1338
11-digit product format
006151338
Labeler code
0615
Product ID
0615-1338_8dcbb073-d3d6-4c00-9e59-6edb07d2c144
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Terazosin
Dosage form
CAPSULE
Route
ORAL
Labeler
NCS HealthCare of KY, Inc dba Vangard Labs
Application
ANDA074823
Marketing category
ANDA
Marketing start
1998-03-30
Marketing end
0000-00-00
Substance
TERAZOSIN HYDROCHLORIDE
Active strength
2 mg/1
Pharmacologic classes
Adrenergic alpha-Antagonists [MoA],alpha-Adrenergic Blocker [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
0615-1338-392022-03-15C16284748780-19d75b9d0-ff0d-f424-e053-dadaa90a57ceaf1c3db8-940a-47bc-b30d-4ae428b9a029
0615-1338-392020-01-31C16284748780-19d75b9d0-ff0d-f424-e053-dadaa90a57ceaf1c3db8-940a-47bc-b30d-4ae428b9a029