Hydralazine Hydrochloride

Product NDC
0615-0516
11-digit product format
006150516
Labeler code
0615
Product ID
0615-0516_1cce9fcb-74f7-4f96-a546-5572b96d4d7c
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Hydralazine Hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
NCS HealthCare of KY, Inc dba Vangard Labs
Application
ANDA087836
Marketing category
ANDA
Marketing start
1982-10-05
Marketing end
0000-00-00
Substance
HYDRALAZINE HYDROCHLORIDE
Active strength
10 mg/1
Pharmacologic classes
Arteriolar Vasodilation [PE],Arteriolar Vasodilator [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
0615-0516-392021-06-14C16284748780-19d75b9d0-4dad-f424-e053-dadaa90a57ce27bb47f9-f177-41c6-8e0c-69331e933278
0615-0516-392020-01-31C16284748780-19d75b9d0-4dad-f424-e053-dadaa90a57ce27bb47f9-f177-41c6-8e0c-69331e933278