Hydralazine Hydrochloride

Product NDC
50090-2610
11-digit product format
500902610
Labeler code
50090
Product ID
50090-2610_2d7ee1f7-be3f-4ba3-b418-9c427972ba7a
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Hydralazine Hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA088467
Marketing category
ANDA
Marketing start
1990-09-30
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

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50090-2610-4EA - Each50090-26106f1780e4-7bb9-474f-8c52-72155d0a7a6012019-04-11
50090-2610-5EA - Each50090-26108ed836db-7853-413c-8b37-ac39bb8ded7412019-04-11