amlodipine and benazepril hydrochloride

Generic: amlodipine and benazepril hydrochloride

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name amlodipine and benazepril hydrochloride
Generic Name amlodipine and benazepril hydrochloride
Labeler a-s medication solutions
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

amlodipine besylate 5 mg/1, benazepril hydrochloride 40 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-3357
Product ID 50090-3357_6fe5e250-1c45-40e2-860e-a8a265e4b378
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202239
Listing Expiration 2026-12-31
Marketing Start 2012-09-05

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 500903357
Hyphenated Format 50090-3357

Supplemental Identifiers

RxCUI
898346 898359
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 and benazepril hydrochloride (source: ndc)
Generic Name amlodipine and benazepril hydrochloride (source: ndc)
Application Number ANDA202239 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
  • 40 mg/1
source: ndc
Packaging
  • 90 CAPSULE in 1 BOTTLE (50090-3357-0)
source: ndc

Packages (1)

50090-3357-0 90 CAPSULE in 1 BOTTLE (50090-3357-0)

Ingredients (2)

amlodipine besylate (5 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": "6fe5e250-1c45-40e2-860e-a8a265e4b378", "openfda": {"unii": ["864V2Q084H", "N1SN99T69T"], "rxcui": ["898346", "898359"], "spl_set_id": ["69a887ab-95cd-4b81-80ee-02e20eebf65b"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE in 1 BOTTLE (50090-3357-0)", "package_ndc": "50090-3357-0", "marketing_start_date": "20180131"}], "brand_name": "Amlodipine and Benazepril Hydrochloride", "product_id": "50090-3357_6fe5e250-1c45-40e2-860e-a8a265e4b378", "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": "50090-3357", "generic_name": "Amlodipine and Benazepril Hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amlodipine and Benazepril Hydrochloride", "active_ingredients": [{"name": "AMLODIPINE BESYLATE", "strength": "5 mg/1"}, {"name": "BENAZEPRIL HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA202239", "marketing_category": "ANDA", "marketing_start_date": "20120905", "listing_expiration_date": "20261231"}