Benazepril Hydrochloride and Hydrochlorothiazide

Product NDC
63629-1809
11-digit product format
636291809
Labeler code
63629
Product ID
63629-1809_c5b571e0-b746-4ca5-9c37-ad63fde6bd5c
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Benazepril Hydrochloride and Hydrochlorothiazide
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA076631
Marketing category
ANDA
Marketing start
2004-02-11
Marketing end
0000-00-00
Substance
BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE
Active strength
10 mg/1; mg/1
Pharmacologic classes
Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS]
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
63629-1809-1EA - Each63629-18094c76017c-c02b-493e-b8f9-3839f5e2f0cc12012-07-24
63629-1809-2EA - Each63629-1809cd179acf-35dd-4541-9a6b-808347a2edd212012-07-24
63629-1809-3EA - Each63629-1809feff3f73-e106-4b81-ae4a-96fa790085cf12015-02-02