amlodipine besylate and benazepril hydrochloride (68180-756)

Drug Facts

Product Profile

Brand Name amlodipine besylate and benazepril hydrochloride

Generic Name amlodipine besylate and benazepril hydrochloride

Labeler lupin pharmaceuticals, inc.

Dosage Form CAPSULE

Routes

ORAL

Active Ingredients

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

Manufacturer

Lupin Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68180-756

Product ID 68180-756_53566d4f-ff40-4815-b922-3416cde56fb1

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 68180756

Hyphenated Format 68180-756

Supplemental Identifiers

RxCUI

898342 898346 898350 898353 898356 898359

UPC

0368180459019

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 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

100 CAPSULE in 1 BOTTLE (68180-756-01)

source: ndc

Packages (1)

68180-756-01 100 CAPSULE in 1 BOTTLE (68180-756-01)

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": "53566d4f-ff40-4815-b922-3416cde56fb1", "openfda": {"upc": ["0368180459019"], "unii": ["864V2Q084H", "N1SN99T69T"], "rxcui": ["898342", "898346", "898350", "898353", "898356", "898359"], "spl_set_id": ["968c611b-43a7-40f0-9ed3-aa67ee88364b"], "manufacturer_name": ["Lupin Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (68180-756-01)", "package_ndc": "68180-756-01", "marketing_start_date": "20100205"}], "brand_name": "Amlodipine Besylate and Benazepril Hydrochloride", "product_id": "68180-756_53566d4f-ff40-4815-b922-3416cde56fb1", "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": "68180-756", "generic_name": "Amlodipine Besylate and Benazepril Hydrochloride", "labeler_name": "Lupin Pharmaceuticals, Inc.", "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"}