atorvastatin calcium

Generic: atorvastatin calcium

Labeler: apotex corp.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name atorvastatin calcium
Generic Name atorvastatin calcium
Labeler apotex corp.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

atorvastatin calcium propylene glycol solvate 40 mg/1

Manufacturer
Apotex Corp.

Identifiers & Regulatory

Product NDC 60505-2580
Product ID 60505-2580_bd45e325-1a2b-b3da-7fd8-58b7ce2a8483
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 605052580
Hyphenated Format 60505-2580

Supplemental Identifiers

RxCUI
259255 617310 617311 617312
UNII
YRZ789OWMI

Packaging Origin

Original Packager
true

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
  • 40 mg/1
source: ndc
Packaging
  • 10 BLISTER PACK in 1 CARTON (60505-2580-0) / 10 TABLET, FILM COATED in 1 BLISTER PACK
  • 30 TABLET, FILM COATED in 1 BOTTLE (60505-2580-3)
  • 500 TABLET, FILM COATED in 1 BOTTLE (60505-2580-5)
  • 4000 TABLET, FILM COATED in 1 BOTTLE (60505-2580-7)
  • 1000 TABLET, FILM COATED in 1 BOTTLE (60505-2580-8)
  • 90 TABLET, FILM COATED in 1 BOTTLE (60505-2580-9)
source: ndc

Packages (6)

Ingredients (1)

atorvastatin calcium propylene glycol solvate (40 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "bd45e325-1a2b-b3da-7fd8-58b7ce2a8483", "openfda": {"unii": ["YRZ789OWMI"], "rxcui": ["259255", "617310", "617311", "617312"], "spl_set_id": ["d9adb9e4-c495-9530-e5e3-7e3b01d53e4c"], "manufacturer_name": ["Apotex Corp."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 CARTON (60505-2580-0)  / 10 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "60505-2580-0", "marketing_start_date": "20120529"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (60505-2580-3)", "package_ndc": "60505-2580-3", "marketing_start_date": "20120529"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (60505-2580-5)", "package_ndc": "60505-2580-5", "marketing_start_date": "20120529"}, {"sample": false, "description": "4000 TABLET, FILM COATED in 1 BOTTLE (60505-2580-7)", "package_ndc": "60505-2580-7", "marketing_start_date": "20120529"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (60505-2580-8)", "package_ndc": "60505-2580-8", "marketing_start_date": "20120529"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (60505-2580-9)", "package_ndc": "60505-2580-9", "marketing_start_date": "20120529"}], "brand_name": "ATORVASTATIN CALCIUM", "product_id": "60505-2580_bd45e325-1a2b-b3da-7fd8-58b7ce2a8483", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "60505-2580", "generic_name": "ATORVASTATIN CALCIUM", "labeler_name": "Apotex Corp.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ATORVASTATIN CALCIUM", "active_ingredients": [{"name": "ATORVASTATIN CALCIUM PROPYLENE GLYCOL SOLVATE", "strength": "40 mg/1"}], "application_number": "ANDA090548", "marketing_category": "ANDA", "marketing_start_date": "20120529", "listing_expiration_date": "20261231"}