atorvastatin calcium

Generic: atorvastatin calcium

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name atorvastatin calcium
Generic Name atorvastatin calcium
Labeler a-s medication solutions
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

atorvastatin calcium propylene glycol solvate 40 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-6440
Product ID 50090-6440_ca11c467-1901-4879-9e30-90c916fe56af
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090548
Listing Expiration 2026-12-31
Marketing Start 2021-08-01

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 500906440
Hyphenated Format 50090-6440

Supplemental Identifiers

RxCUI
617311
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
  • 40 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (50090-6440-0)
  • 90 TABLET, FILM COATED in 1 BOTTLE (50090-6440-1)
  • 100 TABLET, FILM COATED in 1 BOTTLE (50090-6440-2)
source: ndc

Packages (3)

50090-6440-0 30 TABLET, FILM COATED in 1 BOTTLE (50090-6440-0) 50090-6440-1 90 TABLET, FILM COATED in 1 BOTTLE (50090-6440-1) 50090-6440-2 100 TABLET, FILM COATED in 1 BOTTLE (50090-6440-2)

Ingredients (1)

atorvastatin calcium propylene glycol solvate (40 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": "ca11c467-1901-4879-9e30-90c916fe56af", "openfda": {"unii": ["YRZ789OWMI"], "rxcui": ["617311"], "spl_set_id": ["0ab0bcac-10a3-4178-9674-3730683a4183"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-6440-0)", "package_ndc": "50090-6440-0", "marketing_start_date": "20230417"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-6440-1)", "package_ndc": "50090-6440-1", "marketing_start_date": "20230417"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (50090-6440-2)", "package_ndc": "50090-6440-2", "marketing_start_date": "20230417"}], "brand_name": "ATORVASTATIN CALCIUM", "product_id": "50090-6440_ca11c467-1901-4879-9e30-90c916fe56af", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "50090-6440", "generic_name": "ATORVASTATIN CALCIUM", "labeler_name": "A-S Medication Solutions", "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": "20210801", "listing_expiration_date": "20261231"}