amlodipine and atorvastatin

Generic: amlodipine and atorvastatin

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name amlodipine and atorvastatin
Generic Name amlodipine and atorvastatin
Labeler bryant ranch prepack
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

amlodipine besylate 10 mg/1, atorvastatin calcium trihydrate 20 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 72162-2090
Product ID 72162-2090_113d1ccb-d142-4e81-b9c8-5c3ae00b9f56
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA205199
Listing Expiration 2026-12-31
Marketing Start 2020-07-29

Pharmacologic Class

Classes
calcium channel antagonists [moa] calcium channel blocker [epc] cytochrome p450 3a inhibitors [moa] dihydropyridine calcium channel blocker [epc] dihydropyridines [cs] hmg-coa reductase inhibitor [epc] hydroxymethylglutaryl-coa reductase inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 721622090
Hyphenated Format 72162-2090

Supplemental Identifiers

RxCUI
597967
UNII
864V2Q084H 48A5M73Z4Q

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 atorvastatin (source: ndc)
Generic Name amlodipine and atorvastatin (source: ndc)
Application Number ANDA205199 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
  • 20 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (72162-2090-3)
source: ndc

Packages (1)

72162-2090-3 30 TABLET, FILM COATED in 1 BOTTLE (72162-2090-3)

Ingredients (2)

amlodipine besylate (10 mg/1) atorvastatin calcium trihydrate (20 mg/1)

Linked Drug Pages (1)

Amlodipine and Atorvastatin ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "113d1ccb-d142-4e81-b9c8-5c3ae00b9f56", "openfda": {"unii": ["864V2Q084H", "48A5M73Z4Q"], "rxcui": ["597967"], "spl_set_id": ["bed1710f-edd9-488d-855b-603d50ee212c"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72162-2090-3)", "package_ndc": "72162-2090-3", "marketing_start_date": "20240814"}], "brand_name": "Amlodipine and Atorvastatin", "product_id": "72162-2090_113d1ccb-d142-4e81-b9c8-5c3ae00b9f56", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A Inhibitors [MoA]", "Dihydropyridine Calcium Channel Blocker [EPC]", "Dihydropyridines [CS]", "HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "72162-2090", "generic_name": "Amlodipine and Atorvastatin", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amlodipine and Atorvastatin", "active_ingredients": [{"name": "AMLODIPINE BESYLATE", "strength": "10 mg/1"}, {"name": "ATORVASTATIN CALCIUM TRIHYDRATE", "strength": "20 mg/1"}], "application_number": "ANDA205199", "marketing_category": "ANDA", "marketing_start_date": "20200729", "listing_expiration_date": "20261231"}