atorvastatin calcium
Generic: atorvastatin calcium
Labeler: direct_rxDrug Facts
Product Profile
Brand Name
atorvastatin calcium
Generic Name
atorvastatin calcium
Labeler
direct_rx
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
atorvastatin calcium trihydrate 40 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
72189-557
Product ID
72189-557_339eff5f-588e-3a5b-e063-6294a90abed0
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA211933
Listing Expiration
2026-12-31
Marketing Start
2024-06-14
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72189557
Hyphenated Format
72189-557
Supplemental Identifiers
RxCUI
UNII
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
ANDA211933 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 40 mg/1
Packaging
- 30 TABLET, FILM COATED in 1 BOTTLE (72189-557-30)
- 90 TABLET, FILM COATED in 1 BOTTLE (72189-557-90)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "339eff5f-588e-3a5b-e063-6294a90abed0", "openfda": {"unii": ["48A5M73Z4Q"], "rxcui": ["617311"], "spl_set_id": ["1ade00fd-5eb4-f67a-e063-6294a90a9112"], "manufacturer_name": ["Direct_rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72189-557-30)", "package_ndc": "72189-557-30", "marketing_start_date": "20240614"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (72189-557-90)", "package_ndc": "72189-557-90", "marketing_start_date": "20240614"}], "brand_name": "Atorvastatin Calcium", "product_id": "72189-557_339eff5f-588e-3a5b-e063-6294a90abed0", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "72189-557", "generic_name": "Atorvastatin Calcium", "labeler_name": "Direct_rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Atorvastatin Calcium", "active_ingredients": [{"name": "ATORVASTATIN CALCIUM TRIHYDRATE", "strength": "40 mg/1"}], "application_number": "ANDA211933", "marketing_category": "ANDA", "marketing_start_date": "20240614", "listing_expiration_date": "20261231"}