amlodipine besylate
Generic: amlodipine besylate
Labeler: nucare pharmaceuticals,inc.Drug Facts
Product Profile
Brand Name
amlodipine besylate
Generic Name
amlodipine besylate
Labeler
nucare pharmaceuticals,inc.
Dosage Form
TABLET
Routes
Active Ingredients
amlodipine besylate 5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68071-5151
Product ID
68071-5151_1b56238f-81e6-f684-e063-6394a90aa6d2
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA078925
Listing Expiration
2026-12-31
Marketing Start
2010-10-20
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
680715151
Hyphenated Format
68071-5151
Supplemental Identifiers
RxCUI
UPC
UNII
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 (source: ndc)
Generic Name
amlodipine besylate (source: ndc)
Application Number
ANDA078925 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 mg/1
Packaging
- 90 TABLET in 1 BOTTLE (68071-5151-9)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1b56238f-81e6-f684-e063-6394a90aa6d2", "openfda": {"upc": ["0368071515190"], "unii": ["864V2Q084H"], "rxcui": ["197361"], "spl_set_id": ["9c448d87-294e-3325-e053-2a95a90a2299"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (68071-5151-9)", "package_ndc": "68071-5151-9", "marketing_start_date": "20200116"}], "brand_name": "Amlodipine Besylate", "product_id": "68071-5151_1b56238f-81e6-f684-e063-6394a90aa6d2", "dosage_form": "TABLET", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A Inhibitors [MoA]", "Dihydropyridine Calcium Channel Blocker [EPC]", "Dihydropyridines [CS]"], "product_ndc": "68071-5151", "generic_name": "Amlodipine besylate", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amlodipine Besylate", "active_ingredients": [{"name": "AMLODIPINE BESYLATE", "strength": "5 mg/1"}], "application_number": "ANDA078925", "marketing_category": "ANDA", "marketing_start_date": "20101020", "listing_expiration_date": "20261231"}