NDC 50268-109-11 - Benazepril Hydrochloride

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC: 50268-109
Requested NDC: 50268-109-11
Package NDCs from labels: 50268-109-11, 50268-109-15
Manufacturer: AvPAK
Effective date: 2025-09-23
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Benazepril Hydrochloride - AvPAK	AvPAK	2025-09-23	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
50268-109-11	Benazepril Hydrochloride	1 in 1 BLISTER PACK	TABLET	1		11
50268-109-15	Benazepril Hydrochloride	50 in 1 BOX	TABLET	50		11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
50268-109	BENAZEPRIL HYDROCHLORIDE TABLET [AVPAK]	10	Current NDC, Legacy NDC, 2 package rows	20230504_f004d7e2-fc45-8a37-e548-eeaaa327f9b5.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
50268-109-11	EA - Each	50268-109	ac4fecf8-0725-4691-ac80-1ef526c62374	1	2015-04-03
50268-109-15	EA - Each	50268-109	070f951f-e6e0-488e-a022-bf5512baf5f1	1	2014-07-02

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
BENAZEPRIL HYDROCHLORIDE	ACTIVE INGREDIENT	N1SN99T69T	BENAZEPRIL HYDROCHLORIDE TABLET [AVPAK]	2
BENAZEPRILAT	ACTIVE MOIETY	JRM708L703	BENAZEPRIL HYDROCHLORIDE TABLET [AVPAK]	2
Anhydrous Lactose	INACTIVE INGREDIENT	3SY5LH9PMK	BENAZEPRIL HYDROCHLORIDE TABLET [AVPAK]	2
Cellulose, Microcrystalline	INACTIVE INGREDIENT	OP1R32D61U	BENAZEPRIL HYDROCHLORIDE TABLET [AVPAK]	2
Crospovidone	INACTIVE INGREDIENT	68401960MK	BENAZEPRIL HYDROCHLORIDE TABLET [AVPAK]	2
Magnesium Stearate	INACTIVE INGREDIENT	70097M6I30	BENAZEPRIL HYDROCHLORIDE TABLET [AVPAK]	2
Starch, Corn	INACTIVE INGREDIENT	O8232NY3SJ	BENAZEPRIL HYDROCHLORIDE TABLET [AVPAK]	2
Talc	INACTIVE INGREDIENT	7SEV7J4R1U	BENAZEPRIL HYDROCHLORIDE TABLET [AVPAK]	2

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 6 · 109 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Amlodipine Besylate and Benazepril Hydrochloride	AMLODIPINE BESYLATE AND BENAZEPRIL HYDROCHLORIDE	REMEDYREPACK INC.	0f253cac-67ac-4b03-b1a8-f2c345938dda	2026-09-09	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: N1SN99T69T
Amlodipine Besylate and Benazepril Hydrochloride	AMLODIPINE BESYLATE AND BENAZEPRIL HYDROCHLORIDE	REMEDYREPACK INC.	dc206611-5188-40a6-b025-61db41f68a5a	2026-09-09	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: N1SN99T69T
Amlodipine Besylate and Benazepril Hydrochloride	AMLODIPINE BESYLATE AND BENAZEPRIL HYDROCHLORIDE	REMEDYREPACK INC.	2542895b-c8f8-4f21-9e12-f5a7fe17f905	2026-09-09	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: N1SN99T69T
Benazepril Hydrochloride	BENAZEPRIL HYDROCHLORIDE	ANI Pharmaceuticals, Inc.	ff732cfa-9ded-4226-b464-19c90a6865ae	2026-08-19	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 898723 rxcui: 898690 rxcui: 898687 rxcui: 898719 unii: N1SN99T69T
Benazepril Hydrochloride	BENAZEPRIL HYDROCHLORIDE	Amneal Pharmaceuticals of New York LLC	e0ddcfbc-c9d8-45b1-9c11-0d1eff8c1e9e	2026-08-03	Boxed warning, Warnings, Adverse reactions	Exact identifier application number: ANDA076820 ndc (product): 53746-753 ndc (product): 53746-754 ndc (product): 53746-752 ndc (product): 53746-751 rxcui: 898723 rxcui: 898690 rxcui: 898687 rxcui: 898719 spl id: e6ad086e-a030-4d1c-ad5c-6e7568f37439 spl set id: e0ddcfbc-c9d8-45b1-9c11-0d1eff8c1e9e unii: N1SN99T69T
Benazepril Hydrochloride	BENAZEPRIL HYDROCHLORIDE	REMEDYREPACK INC.	afd616b9-0c75-48be-862d-5ac18364fd9d	2026-07-17	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 898719 unii: N1SN99T69T
Amlodipine and Benazepril Hydrochloride	AMLODIPINE AND BENAZEPRIL HYDROCHLORIDE	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	27b0c628-820a-48bf-a411-86c0ebd4cc8d	2026-06-29	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: N1SN99T69T
Benazepril Hydrochloride	BENAZEPRIL HYDROCHLORIDE	Bryant Ranch Prepack	58977ec4-36ea-4d81-a8f0-7298425cbc84	2026-06-05	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 898719 unii: N1SN99T69T
Benazepril Hydrochloride	BENAZEPRIL HYDROCHLORIDE	PD-Rx Pharmaceuticals, Inc.	5de2ea54-877d-46e9-b4c2-bf1ab9d0f19c	2026-05-14	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 898719 unii: N1SN99T69T
Amlodipine Besylate and Benazepril Hydrochloride	AMLODIPINE BESYLATE AND BENAZEPRIL HYDROCHLORIDE	A-S Medication Solutions	c695f95d-6064-4a22-84ba-c8e62477b3a7	2026-05-11	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: N1SN99T69T
Benazepril Hydrochloride	BENAZEPRIL HYDROCHLORIDE	REMEDYREPACK INC.	6dc12ab4-2282-412f-8aa1-46ec5fbbab8f	2026-04-27	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 898690 unii: N1SN99T69T
Amlodipine Besylate and Benazepril Hydrochloride	AMLODIPINE BESYLATE AND BENAZEPRIL HYDROCHLORIDE	Bryant Ranch Prepack	318b3273-e8f7-416c-b371-10c56fa8e0fd	2026-04-20	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: N1SN99T69T
Benazepril Hydrochloride	BENAZEPRIL HYDROCHLORIDE	Cardinal Health 107, LLC	f265e6dd-f47e-4511-9468-282184bcd1b1	2026-04-13	Boxed warning, Warnings, Adverse reactions	Exact identifier application number: ANDA076820 rxcui: 898690 rxcui: 898687 unii: N1SN99T69T
Amlodipine Besylate and Benazepril Hydrochloride	AMLODIPINE BESYLATE AND BENAZEPRIL HYDROCHLORIDE	Amneal Pharmaceuticals NY LLC	856a8cdc-57cc-4355-966d-986bbc5fa6e6	2026-03-31	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: N1SN99T69T
Amlodipine Besylate and Benazepril Hydrochloride	AMLODIPINE BESYLATE AND BENAZEPRIL HYDROCHLORIDE	PD-Rx Pharmaceuticals, Inc.	5f7a4bd1-8083-46ca-95f2-e8c476b5367c	2026-03-27	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: N1SN99T69T
Amlodipine Besylate and Benazepril Hydrochloride	AMLODIPINE BESYLATE AND BENAZEPRIL HYDROCHLORIDE	PD-Rx Pharmaceuticals, Inc.	ff807933-7433-4f8c-9d09-02a57e51d0fc	2026-03-20	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: N1SN99T69T
Benazepril Hydrochloride	BENAZEPRIL HYDROCHLORIDE	Preferred Pharmaceuticals Inc.	01a3c9f6-41aa-47a7-8c56-5462c6b54416	2026-03-19	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 898723 unii: N1SN99T69T
Benazepril Hydrochloride	BENAZEPRIL HYDROCHLORIDE	Preferred Pharmaceuticals, Inc.	032ea0f7-3304-4778-b3a6-6125ea7537ab	2026-03-19	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 898690 rxcui: 898687 unii: N1SN99T69T
Benazepril Hydrochloride	BENAZEPRIL HYDROCHLORIDE	Aurobindo Pharma Limited	09e383a8-e912-4cf7-8fb3-05545af80dd0	2026-03-13	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 898690 rxcui: 898687 rxcui: 898719 unii: N1SN99T69T
Amlodipine Besylate and Benazepril Hydrochloride	AMLODIPINE BESYLATE AND BENAZEPRIL HYDROCHLORIDE	Bryant Ranch Prepack	f16e04b5-57b9-49cc-811b-07d85ccb5d9f	2026-03-06	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: N1SN99T69T

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.