Spironolactone

Product NDC
0615-5592
11-digit product format
006155592
Labeler code
0615
Product ID
0615-5592_c811c81f-84d9-4d55-bbd4-2b30a6e5a32d
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
spironolactone
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
NCS HealthCare of KY, Inc dba Vangard Labs
Application
ANDA040424
Marketing category
ANDA
Marketing start
2001-08-20
Marketing end
0000-00-00
Substance
SPIRONOLACTONE
Active strength
50 mg/1
Pharmacologic classes
Aldosterone Antagonist [EPC],Aldosterone Antagonists [MoA]
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
0615-5592-392021-09-03C16284748780-19d75b9d0-e15b-f424-e053-dadaa90a57ce7d16b436-c76c-4ac8-b36a-149a14faecab
0615-5592-392020-01-31C16284748780-19d75b9d0-e15b-f424-e053-dadaa90a57ce7d16b436-c76c-4ac8-b36a-149a14faecab