Hydralazine Hydrochloride

Product NDC
0904-6443
11-digit product format
009046443
Labeler code
0904
Product ID
0904-6443_512fa4b6-6ff4-4eb6-a4e5-8a7d55fda758
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Hydralazine Hydrochloride
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Major Pharmaceuticals
Application
ANDA086242
Marketing category
ANDA
Marketing start
2015-05-14
Marketing end
0000-00-00
Substance
HYDRALAZINE HYDROCHLORIDE
Active strength
100 mg/1
Pharmacologic classes
Arteriolar Vasodilation [PE], Arteriolar Vasodilator [EPC]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0904-6443-61EA - Each0904-6443610478d9-bc76-4d0a-9c2f-daadd5d38e9e12019-04-11

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0904-6443HYDRALAZINE HYDROCHLORIDE TABLET, FILM COATED [MAJOR PHARMACEUTICALS]9Legacy NDC20240629_7dc7c11b-ac51-4db3-ac6a-708c676a8859.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0904-6443-10009046443101000 TABLET, FILM COATED in 1 BOTTLE (0904-6443-10) 2015-05-140000-00-00NoNoCurrent
0904-6443-6100904644361100 BLISTER PACK in 1 CARTON (0904-6443-61) > 1 TABLET, FILM COATED in 1 BLISTER PACK100 blister pack2015-05-140000-00-00NoNoCurrent