atorvastatin calcium

Generic: atorvastatin calcium

Labeler: northwind health company, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name atorvastatin calcium
Generic Name atorvastatin calcium
Labeler northwind health company, llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

atorvastatin calcium propylene glycol solvate 20 mg/1

Manufacturer
Northwind Health Company, LLC

Identifiers & Regulatory

Product NDC 51655-920
Product ID 51655-920_49743995-7fc8-3d7a-e063-6394a90a0755
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090548
Listing Expiration 2027-12-31
Marketing Start 2014-03-11

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 51655920
Hyphenated Format 51655-920

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
  • 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-920-26)
  • 30 TABLET, FILM COATED in 1 BOTTLE (51655-920-30)
  • 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-920-83)
source: ndc

Packages (3)

51655-920-26 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-920-26) 51655-920-30 30 TABLET, FILM COATED in 1 BOTTLE (51655-920-30) 51655-920-83 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-920-83)

Ingredients (1)

atorvastatin calcium propylene glycol solvate (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": "49743995-7fc8-3d7a-e063-6394a90a0755", "openfda": {"unii": ["YRZ789OWMI"], "rxcui": ["617310"], "spl_set_id": ["0e10adb3-8d3a-412f-ae56-d9b9bed4641f"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-920-26)", "package_ndc": "51655-920-26", "marketing_start_date": "20220817"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (51655-920-30)", "package_ndc": "51655-920-30", "marketing_start_date": "20140311"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-920-83)", "package_ndc": "51655-920-83", "marketing_start_date": "20230105"}], "brand_name": "ATORVASTATIN CALCIUM", "product_id": "51655-920_49743995-7fc8-3d7a-e063-6394a90a0755", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "51655-920", "generic_name": "ATORVASTATIN CALCIUM", "labeler_name": "Northwind Health Company, LLC", "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": "20140311", "listing_expiration_date": "20271231"}