amlodipine and benazepril hydrochloride (23155-925)

Drug Facts

Product Profile

Brand Name amlodipine and benazepril hydrochloride

Generic Name amlodipine and benazepril hydrochloride

Labeler heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.

Dosage Form CAPSULE

Routes

ORAL

Active Ingredients

amlodipine besylate 10 mg/1, benazepril hydrochloride 40 mg/1

Manufacturer

Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 23155-925

Product ID 23155-925_e2f5c585-ebd4-430f-bbc7-37ba524bda85

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA091431

Listing Expiration 2027-12-31

Marketing Start 2025-10-15

Pharmacologic Class

Classes

angiotensin converting enzyme inhibitor [epc] angiotensin-converting enzyme inhibitors [moa] calcium channel antagonists [moa] calcium channel blocker [epc] cytochrome p450 3a inhibitors [moa] decreased blood pressure [pe] dihydropyridine calcium channel blocker [epc] dihydropyridines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 23155925

Hyphenated Format 23155-925

Supplemental Identifiers

RxCUI

898346 898350 898356

UPC

0323155925012 0323155920109 0323155922059 0323155925104 0323155920017 0323155922103 0323155925050 0323155920055 0323155922011

UNII

864V2Q084H N1SN99T69T

Packaging Origin

Original Packager

true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name amlodipine and benazepril hydrochloride (source: ndc)

Generic Name amlodipine and benazepril hydrochloride (source: ndc)

Application Number ANDA091431 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

10 mg/1
40 mg/1

source: ndc

Packaging

100 CAPSULE in 1 BOTTLE (23155-925-01)
500 CAPSULE in 1 BOTTLE (23155-925-05)
1000 CAPSULE in 1 BOTTLE (23155-925-10)

source: ndc

Packages (3)

23155-925-01 100 CAPSULE in 1 BOTTLE (23155-925-01) 23155-925-05 500 CAPSULE in 1 BOTTLE (23155-925-05) 23155-925-10 1000 CAPSULE in 1 BOTTLE (23155-925-10)

Ingredients (2)

amlodipine besylate (10 mg/1) benazepril hydrochloride (40 mg/1)

Linked Drug Pages (1)

Amlodipine and Benazepril Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["ORAL"], "spl_id": "e2f5c585-ebd4-430f-bbc7-37ba524bda85", "openfda": {"upc": ["0323155925012", "0323155920109", "0323155922059", "0323155925104", "0323155920017", "0323155922103", "0323155925050", "0323155920055", "0323155922011"], "unii": ["864V2Q084H", "N1SN99T69T"], "rxcui": ["898346", "898350", "898356"], "spl_set_id": ["27b0c628-820a-48bf-a411-86c0ebd4cc8d"], "manufacturer_name": ["Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (23155-925-01)", "package_ndc": "23155-925-01", "marketing_start_date": "20251015"}, {"sample": false, "description": "500 CAPSULE in 1 BOTTLE (23155-925-05)", "package_ndc": "23155-925-05", "marketing_start_date": "20251015"}, {"sample": false, "description": "1000 CAPSULE in 1 BOTTLE (23155-925-10)", "package_ndc": "23155-925-10", "marketing_start_date": "20251015"}], "brand_name": "Amlodipine and Benazepril Hydrochloride", "product_id": "23155-925_e2f5c585-ebd4-430f-bbc7-37ba524bda85", "dosage_form": "CAPSULE", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A Inhibitors [MoA]", "Decreased Blood Pressure [PE]", "Dihydropyridine Calcium Channel Blocker [EPC]", "Dihydropyridines [CS]"], "product_ndc": "23155-925", "generic_name": "Amlodipine and Benazepril Hydrochloride", "labeler_name": "Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amlodipine and Benazepril Hydrochloride", "active_ingredients": [{"name": "AMLODIPINE BESYLATE", "strength": "10 mg/1"}, {"name": "BENAZEPRIL HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA091431", "marketing_category": "ANDA", "marketing_start_date": "20251015", "listing_expiration_date": "20271231"}