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 10 mg/1, benazepril hydrochloride 20 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-7361
Product ID 50090-7361_90815557-bb3d-4587-b552-b255bf040c14
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 500907361
Hyphenated Format 50090-7361

Supplemental Identifiers

RxCUI
898342
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
  • 10 mg/1
  • 20 mg/1
source: ndc
Packaging
  • 30 CAPSULE in 1 BOTTLE (50090-7361-0)
  • 90 CAPSULE in 1 BOTTLE (50090-7361-1)
source: ndc

Packages (2)

50090-7361-0 30 CAPSULE in 1 BOTTLE (50090-7361-0) 50090-7361-1 90 CAPSULE in 1 BOTTLE (50090-7361-1)

Ingredients (2)

amlodipine besylate (10 mg/1) benazepril hydrochloride (20 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": "90815557-bb3d-4587-b552-b255bf040c14", "openfda": {"unii": ["864V2Q084H", "N1SN99T69T"], "rxcui": ["898342"], "spl_set_id": ["b6eb5283-8e07-47b8-b440-fe72859d8bcc"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (50090-7361-0)", "package_ndc": "50090-7361-0", "marketing_start_date": "20241017"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (50090-7361-1)", "package_ndc": "50090-7361-1", "marketing_start_date": "20241017"}], "brand_name": "Amlodipine and Benazepril Hydrochloride", "product_id": "50090-7361_90815557-bb3d-4587-b552-b255bf040c14", "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": "50090-7361", "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": "10 mg/1"}, {"name": "BENAZEPRIL HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA202239", "marketing_category": "ANDA", "marketing_start_date": "20120905", "listing_expiration_date": "20261231"}