amlodipine besylate and benazepril hydrochloride
Generic: amlodipine besylate and benazepril hydrochloride
Labeler: dr.reddy's laboratories limitedDrug Facts
Product Profile
Brand Name
amlodipine besylate and benazepril hydrochloride
Generic Name
amlodipine besylate and benazepril hydrochloride
Labeler
dr.reddy's laboratories limited
Dosage Form
CAPSULE
Routes
Active Ingredients
amlodipine besylate 10 mg/1, benazepril hydrochloride 40 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
55111-586
Product ID
55111-586_2b57e667-c854-2ed1-32f9-b06c6fea1930
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA090149
Listing Expiration
2026-12-31
Marketing Start
2011-07-05
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
55111586
Hyphenated Format
55111-586
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
ANDA090149 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/1
- 40 mg/1
Packaging
- 100 CAPSULE in 1 BOTTLE (55111-586-01)
- 500 CAPSULE in 1 BOTTLE (55111-586-05)
- 30 CAPSULE in 1 BOTTLE (55111-586-30)
Packages (3)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2b57e667-c854-2ed1-32f9-b06c6fea1930", "openfda": {"unii": ["864V2Q084H", "N1SN99T69T"], "rxcui": ["898346", "898359"], "spl_set_id": ["f12f18bb-7ddb-e7dc-4edd-32f4ac212bca"], "manufacturer_name": ["Dr.Reddy's Laboratories Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (55111-586-01)", "package_ndc": "55111-586-01", "marketing_start_date": "20110705"}, {"sample": false, "description": "500 CAPSULE in 1 BOTTLE (55111-586-05)", "package_ndc": "55111-586-05", "marketing_start_date": "20110705"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE (55111-586-30)", "package_ndc": "55111-586-30", "marketing_start_date": "20110705"}], "brand_name": "Amlodipine Besylate and Benazepril Hydrochloride", "product_id": "55111-586_2b57e667-c854-2ed1-32f9-b06c6fea1930", "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": "55111-586", "generic_name": "Amlodipine Besylate and Benazepril Hydrochloride", "labeler_name": "Dr.Reddy's Laboratories Limited", "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": "40 mg/1"}], "application_number": "ANDA090149", "marketing_category": "ANDA", "marketing_start_date": "20110705", "listing_expiration_date": "20261231"}