amlodipine besylate and benazepril hydrochloride (50090-5404)

Drug Facts

Product Profile

Brand Name amlodipine besylate and benazepril hydrochloride

Generic Name amlodipine besylate and benazepril hydrochloride

Labeler a-s medication solutions

Dosage Form CAPSULE

Routes

ORAL

Active Ingredients

amlodipine besylate 5 mg/1, benazepril hydrochloride 10 mg/1

Manufacturer

A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-5404

Product ID 50090-5404_c51ade0a-9507-4c41-afbf-4e33d0e30eaf

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA078466

Listing Expiration 2026-12-31

Marketing Start 2010-02-05

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 500905404

Hyphenated Format 50090-5404

Supplemental Identifiers

RxCUI

898353

UNII

864V2Q084H N1SN99T69T

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 besylate and benazepril hydrochloride (source: ndc)

Generic Name amlodipine besylate and benazepril hydrochloride (source: ndc)

Application Number ANDA078466 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

5 mg/1
10 mg/1

source: ndc

Packaging

30 CAPSULE in 1 BOTTLE (50090-5404-0)

source: ndc

Packages (1)

50090-5404-0 30 CAPSULE in 1 BOTTLE (50090-5404-0)

Ingredients (2)

amlodipine besylate (5 mg/1) benazepril hydrochloride (10 mg/1)

Linked Drug Pages (1)

Amlodipine Besylate and Benazepril Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["ORAL"], "spl_id": "c51ade0a-9507-4c41-afbf-4e33d0e30eaf", "openfda": {"unii": ["864V2Q084H", "N1SN99T69T"], "rxcui": ["898353"], "spl_set_id": ["3ad66075-0875-4703-9d21-a424b5ab892a"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (50090-5404-0)", "package_ndc": "50090-5404-0", "marketing_start_date": "20201209"}], "brand_name": "Amlodipine Besylate and Benazepril Hydrochloride", "product_id": "50090-5404_c51ade0a-9507-4c41-afbf-4e33d0e30eaf", "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": "50090-5404", "generic_name": "Amlodipine Besylate and Benazepril Hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amlodipine Besylate and Benazepril Hydrochloride", "active_ingredients": [{"name": "AMLODIPINE BESYLATE", "strength": "5 mg/1"}, {"name": "BENAZEPRIL HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA078466", "marketing_category": "ANDA", "marketing_start_date": "20100205", "listing_expiration_date": "20261231"}