amlodipine besylate and benazepril hydrochloride

Generic: amlodipine besylate and benazepril hydrochloride

Labeler: northwind health company, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name amlodipine besylate and benazepril hydrochloride
Generic Name amlodipine besylate and benazepril hydrochloride
Labeler northwind health company, llc
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

amlodipine besylate 10 mg/1, benazepril hydrochloride 20 mg/1

Manufacturer
Northwind Health Company, LLC

Identifiers & Regulatory

Product NDC 82868-041
Product ID 82868-041_46dcb5ee-e8ae-9a1a-e063-6294a90a5fa5
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077183
Listing Expiration 2026-12-31
Marketing Start 2024-01-19

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 82868041
Hyphenated Format 82868-041

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 besylate and benazepril hydrochloride (source: ndc)
Generic Name amlodipine besylate and benazepril hydrochloride (source: ndc)
Application Number ANDA077183 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
  • 20 mg/1
source: ndc
Packaging
  • 90 CAPSULE in 1 BOTTLE, PLASTIC (82868-041-90)
source: ndc

Packages (1)

82868-041-90 90 CAPSULE in 1 BOTTLE, PLASTIC (82868-041-90)

Ingredients (2)

amlodipine besylate (10 mg/1) benazepril hydrochloride (20 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": "46dcb5ee-e8ae-9a1a-e063-6294a90a5fa5", "openfda": {"unii": ["864V2Q084H", "N1SN99T69T"], "rxcui": ["898342"], "spl_set_id": ["106c08c2-90eb-6bc0-e063-6294a90a5a23"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE in 1 BOTTLE, PLASTIC (82868-041-90)", "package_ndc": "82868-041-90", "marketing_start_date": "20240119"}], "brand_name": "Amlodipine Besylate and Benazepril Hydrochloride", "product_id": "82868-041_46dcb5ee-e8ae-9a1a-e063-6294a90a5fa5", "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": "82868-041", "generic_name": "Amlodipine Besylate and Benazepril Hydrochloride", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amlodipine Besylate and Benazepril Hydrochloride", "active_ingredients": [{"name": "AMLODIPINE BESYLATE", "strength": "10 mg/1"}, {"name": "BENAZEPRIL HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA077183", "marketing_category": "ANDA", "marketing_start_date": "20240119", "listing_expiration_date": "20261231"}