amlodipine and benazepril hydrochloride

Generic: amlodipine and benazepril hydrochloride

Labeler: golden state medical supply, inc.
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 golden state medical supply, inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

amlodipine besylate 10 mg/1, benazepril hydrochloride 40 mg/1

Manufacturer
Golden State Medical Supply, Inc.

Identifiers & Regulatory

Product NDC 84677-013
Product ID 84677-013_4b35268c-9ae9-b3e8-e063-6394a90a9a86
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA091431
Listing Expiration 2027-12-31
Marketing Start 2013-12-30

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 84677013
Hyphenated Format 84677-013

Supplemental Identifiers

RxCUI
898346
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 ANDA091431 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
  • 40 mg/1
source: ndc
Packaging
  • 100 CAPSULE in 1 BOTTLE (84677-013-01)
source: ndc

Packages (1)

84677-013-01 100 CAPSULE in 1 BOTTLE (84677-013-01)

Ingredients (2)

amlodipine besylate (10 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": "4b35268c-9ae9-b3e8-e063-6394a90a9a86", "openfda": {"unii": ["864V2Q084H", "N1SN99T69T"], "rxcui": ["898346"], "spl_set_id": ["47acdbff-b538-9edc-e063-6394a90a3e3b"], "manufacturer_name": ["Golden State Medical Supply, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (84677-013-01)", "package_ndc": "84677-013-01", "marketing_start_date": "20251028"}], "brand_name": "Amlodipine and Benazepril Hydrochloride", "product_id": "84677-013_4b35268c-9ae9-b3e8-e063-6394a90a9a86", "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": "84677-013", "generic_name": "Amlodipine and Benazepril Hydrochloride", "labeler_name": "Golden State Medical Supply, Inc.", "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": "40 mg/1"}], "application_number": "ANDA091431", "marketing_category": "ANDA", "marketing_start_date": "20131230", "listing_expiration_date": "20271231"}