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 20 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-7386
Product ID 50090-7386_e8fb0195-46da-4f25-8cfd-b925a95c2415
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA214344
Listing Expiration 2027-12-31
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 500907386
Hyphenated Format 50090-7386

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 ANDA214344 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (50090-7386-0)
  • 90 TABLET, FILM COATED in 1 BOTTLE (50090-7386-1)
  • 100 TABLET, FILM COATED in 1 BOTTLE (50090-7386-2)
source: ndc

Packages (3)

50090-7386-0 30 TABLET, FILM COATED in 1 BOTTLE (50090-7386-0) 50090-7386-1 90 TABLET, FILM COATED in 1 BOTTLE (50090-7386-1) 50090-7386-2 100 TABLET, FILM COATED in 1 BOTTLE (50090-7386-2)

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": "e8fb0195-46da-4f25-8cfd-b925a95c2415", "openfda": {"unii": ["48A5M73Z4Q"], "rxcui": ["617310"], "spl_set_id": ["db32eb1a-d282-47df-afa2-f250e3c67e71"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-7386-0)", "package_ndc": "50090-7386-0", "marketing_start_date": "20241021"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-7386-1)", "package_ndc": "50090-7386-1", "marketing_start_date": "20241021"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (50090-7386-2)", "package_ndc": "50090-7386-2", "marketing_start_date": "20241021"}], "brand_name": "ATORVASTATIN CALCIUM", "product_id": "50090-7386_e8fb0195-46da-4f25-8cfd-b925a95c2415", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "50090-7386", "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": "20 mg/1"}], "application_number": "ANDA214344", "marketing_category": "ANDA", "marketing_start_date": "20230912", "listing_expiration_date": "20271231"}