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 trihydrate 80 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-7358
Product ID 50090-7358_7cd74eaa-ad0d-4324-9ec4-ca851ac3d0a3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA214344
Listing Expiration 2026-12-31
Marketing Start 2023-09-12

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 500907358
Hyphenated Format 50090-7358

Supplemental Identifiers

RxCUI
259255
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 ANDA214344 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 80 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (50090-7358-0)
  • 90 TABLET, FILM COATED in 1 BOTTLE (50090-7358-1)
  • 100 TABLET, FILM COATED in 1 BOTTLE (50090-7358-2)
source: ndc

Packages (3)

50090-7358-0 30 TABLET, FILM COATED in 1 BOTTLE (50090-7358-0) 50090-7358-1 90 TABLET, FILM COATED in 1 BOTTLE (50090-7358-1) 50090-7358-2 100 TABLET, FILM COATED in 1 BOTTLE (50090-7358-2)

Ingredients (1)

atorvastatin calcium trihydrate (80 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": "7cd74eaa-ad0d-4324-9ec4-ca851ac3d0a3", "openfda": {"unii": ["48A5M73Z4Q"], "rxcui": ["259255"], "spl_set_id": ["a4185ea4-8fc1-4af5-99b1-6e49f0c46463"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-7358-0)", "package_ndc": "50090-7358-0", "marketing_start_date": "20241017"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-7358-1)", "package_ndc": "50090-7358-1", "marketing_start_date": "20241017"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (50090-7358-2)", "package_ndc": "50090-7358-2", "marketing_start_date": "20241017"}], "brand_name": "ATORVASTATIN CALCIUM", "product_id": "50090-7358_7cd74eaa-ad0d-4324-9ec4-ca851ac3d0a3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "50090-7358", "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 TRIHYDRATE", "strength": "80 mg/1"}], "application_number": "ANDA214344", "marketing_category": "ANDA", "marketing_start_date": "20230912", "listing_expiration_date": "20261231"}