Hydralazine Hydrochloride

Product NDC
35356-944
11-digit product format
353560944
Labeler code
35356
Product ID
35356-944_aecda0b9-bc01-49be-b631-ea7d074c2560
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Hydralazine Hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
Lake Erie Medical DBA Quality Care Products LLC
Application
ANDA090527
Marketing category
ANDA
Marketing start
2009-06-01
Marketing end
0000-00-00
Substance
HYDRALAZINE HYDROCHLORIDE
Active strength
25 mg/1
Pharmacologic classes
Arteriolar Vasodilation [PE],Arteriolar Vasodilator [EPC]
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
35356-944-60EA - Each35356-9440568ee3a-32ed-4f1a-a1b8-c6ba574500e612013-09-04