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 trihydrate 20 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 72162-1555
Product ID 72162-1555_4577f7c3-f68a-45fb-927b-c3caabce8f30
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA205519
Listing Expiration 2027-12-31
Marketing Start 2016-05-19

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 721621555
Hyphenated Format 72162-1555

Supplemental Identifiers

RxCUI
617310
UNII
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 atorvastatin calcium (source: ndc)
Generic Name atorvastatin calcium (source: ndc)
Application Number ANDA205519 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 500 TABLET, FILM COATED in 1 BOTTLE (72162-1555-5)
  • 90 TABLET, FILM COATED in 1 BOTTLE (72162-1555-9)
source: ndc

Packages (2)

72162-1555-5 500 TABLET, FILM COATED in 1 BOTTLE (72162-1555-5) 72162-1555-9 90 TABLET, FILM COATED in 1 BOTTLE (72162-1555-9)

Ingredients (1)

atorvastatin calcium trihydrate (20 mg/1)

Linked Drug Pages (1)

ATORVASTATIN CALCIUM ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4577f7c3-f68a-45fb-927b-c3caabce8f30", "openfda": {"unii": ["48A5M73Z4Q"], "rxcui": ["617310"], "spl_set_id": ["5b9a5a36-7814-4d19-b146-01e819676ae2"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (72162-1555-5)", "package_ndc": "72162-1555-5", "marketing_start_date": "20160519"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (72162-1555-9)", "package_ndc": "72162-1555-9", "marketing_start_date": "20160519"}], "brand_name": "ATORVASTATIN CALCIUM", "product_id": "72162-1555_4577f7c3-f68a-45fb-927b-c3caabce8f30", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "72162-1555", "generic_name": "ATORVASTATIN CALCIUM", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ATORVASTATIN CALCIUM", "active_ingredients": [{"name": "ATORVASTATIN CALCIUM TRIHYDRATE", "strength": "20 mg/1"}], "application_number": "ANDA205519", "marketing_category": "ANDA", "marketing_start_date": "20160519", "listing_expiration_date": "20271231"}