Benazepril hydrochloride

Product NDC: 51655-067
11-digit product format: 516550067
Labeler code: 51655
Product ID: 51655-067_f3da3837-01b1-49df-8a12-82587391d24a
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Benazepril hydrochloride
Dosage form: TABLET, FILM COATED
Route: ORAL
Labeler: Northwind Pharmaceuticals
Application: ANDA076118
Marketing category: ANDA
Marketing start: 2014-05-30
Marketing end: 0000-00-00
Substance: BENAZEPRIL HYDROCHLORIDE
Active strength: 20 mg/1
Pharmacologic classes: Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE]
NDC exclude flag: E
Listing certified through: 2018-12-31
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
51655-067-52	2026-01-08	C162847	48780-1	9d75b9d0-7315-f424-e053-dadaa90a57ce	22830fc9-88fc-484e-924e-28809ef46034
51655-067-52	2020-01-31	C162847	48780-1	9d75b9d0-7315-f424-e053-dadaa90a57ce	22830fc9-88fc-484e-924e-28809ef46034

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version	Uploaded
BENAZEPRIL HYDROCHLORIDE	ACTIVE INGREDIENT	N1SN99T69T	BENAZEPRIL HYDROCHLORIDE TABLET, FILM COATED [NORTHWIND PHARMACEUTICALS]	1
BENAZEPRILAT	ACTIVE MOIETY	JRM708L703	BENAZEPRIL HYDROCHLORIDE TABLET, FILM COATED [NORTHWIND PHARMACEUTICALS]	1

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
51655-067	BENAZEPRIL HYDROCHLORIDE TABLET, FILM COATED [NORTHWIND PHARMACEUTICALS]	1	Legacy NDC	20140616_22830fc9-88fc-484e-924e-28809ef46034.zip