atorvastatin calcium

Generic: atorvastatin calcium

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

Drug Facts

Product Profile

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

atorvastatin calcium propylene glycol solvate 20 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-1051
Product ID 71335-1051_7dd59be7-0b85-434a-925b-e2b9926f9e45
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090548
Listing Expiration 2026-12-31
Marketing Start 2012-05-29

Pharmacologic Class

Classes
hmg-coa reductase inhibitor [epc] hydroxymethylglutaryl-coa reductase inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713351051
Hyphenated Format 71335-1051

Supplemental Identifiers

RxCUI
617310
UNII
YRZ789OWMI

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 atorvastatin calcium (source: ndc)
Generic Name atorvastatin calcium (source: ndc)
Application Number ANDA090548 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (71335-1051-1)
  • 60 TABLET, FILM COATED in 1 BOTTLE (71335-1051-2)
  • 90 TABLET, FILM COATED in 1 BOTTLE (71335-1051-3)
  • 9 TABLET, FILM COATED in 1 BOTTLE (71335-1051-4)
  • 28 TABLET, FILM COATED in 1 BOTTLE (71335-1051-5)
  • 20 TABLET, FILM COATED in 1 BOTTLE (71335-1051-6)
  • 180 TABLET, FILM COATED in 1 BOTTLE (71335-1051-7)
  • 100 TABLET, FILM COATED in 1 BOTTLE (71335-1051-8)
  • 7 TABLET, FILM COATED in 1 BOTTLE (71335-1051-9)
source: ndc

Packages (9)

Ingredients (1)

atorvastatin calcium propylene glycol solvate (20 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "7dd59be7-0b85-434a-925b-e2b9926f9e45", "openfda": {"unii": ["YRZ789OWMI"], "rxcui": ["617310"], "spl_set_id": ["694a6a7f-9d46-46b0-9329-ad8c2bd5e403"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-1051-1)", "package_ndc": "71335-1051-1", "marketing_start_date": "20190104"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-1051-2)", "package_ndc": "71335-1051-2", "marketing_start_date": "20241209"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-1051-3)", "package_ndc": "71335-1051-3", "marketing_start_date": "20190206"}, {"sample": false, "description": "9 TABLET, FILM COATED in 1 BOTTLE (71335-1051-4)", "package_ndc": "71335-1051-4", "marketing_start_date": "20241209"}, {"sample": false, "description": "28 TABLET, FILM COATED in 1 BOTTLE (71335-1051-5)", "package_ndc": "71335-1051-5", "marketing_start_date": "20241209"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (71335-1051-6)", "package_ndc": "71335-1051-6", "marketing_start_date": "20241209"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE (71335-1051-7)", "package_ndc": "71335-1051-7", "marketing_start_date": "20241209"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (71335-1051-8)", "package_ndc": "71335-1051-8", "marketing_start_date": "20241209"}, {"sample": false, "description": "7 TABLET, FILM COATED in 1 BOTTLE (71335-1051-9)", "package_ndc": "71335-1051-9", "marketing_start_date": "20241209"}], "brand_name": "ATORVASTATIN CALCIUM", "product_id": "71335-1051_7dd59be7-0b85-434a-925b-e2b9926f9e45", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "71335-1051", "generic_name": "ATORVASTATIN CALCIUM", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ATORVASTATIN CALCIUM", "active_ingredients": [{"name": "ATORVASTATIN CALCIUM PROPYLENE GLYCOL SOLVATE", "strength": "20 mg/1"}], "application_number": "ANDA090548", "marketing_category": "ANDA", "marketing_start_date": "20120529", "listing_expiration_date": "20261231"}