atorvastatin calcium

Generic: atorvastatin calcium

Labeler: direct rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name atorvastatin calcium
Generic Name atorvastatin calcium
Labeler direct rx
Dosage Form TABLET
Routes
ORAL
Active Ingredients

atorvastatin calcium trihydrate 40 mg/1

Manufacturer
DIRECT RX

Identifiers & Regulatory

Product NDC 72189-239
Product ID 72189-239_2c283f9f-1dbb-4a4c-e063-6394a90a7953
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204991
Listing Expiration 2026-12-31
Marketing Start 2021-09-20

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 72189239
Hyphenated Format 72189-239

Supplemental Identifiers

RxCUI
617312
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 ANDA204991 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE (72189-239-90)
source: ndc

Packages (1)

Ingredients (1)

atorvastatin calcium trihydrate (40 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2c283f9f-1dbb-4a4c-e063-6394a90a7953", "openfda": {"unii": ["48A5M73Z4Q"], "rxcui": ["617312"], "spl_set_id": ["c3b70f79-45a3-0869-e053-2a95a90a3cdb"], "manufacturer_name": ["DIRECT RX"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (72189-239-90)", "package_ndc": "72189-239-90", "marketing_start_date": "20210920"}], "brand_name": "ATORVASTATIN CALCIUM", "product_id": "72189-239_2c283f9f-1dbb-4a4c-e063-6394a90a7953", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "72189-239", "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": "ANDA204991", "marketing_category": "ANDA", "marketing_start_date": "20210920", "listing_expiration_date": "20261231"}