Atorvastatin Calcium

Generic: Atorvastatin Calcium

Labeler: Preferred Pharmaceuticals Inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Active

Drug Facts

Product Profile

Brand Name Atorvastatin Calcium
Generic Name Atorvastatin Calcium
Labeler Preferred Pharmaceuticals Inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

ATORVASTATIN CALCIUM TRIHYDRATE 10 mg/1

Identifiers & Regulatory

Product NDC 68788-7900
Product ID 68788-7900_d7038238-24d7-498e-988a-0448f095eb8d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209288
Listing Expiration 2026-12-31
Marketing Start 2021-05-14

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 687887900
Hyphenated Format 68788-7900

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 ANDA209288 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (68788-7900-1)
  • 30 TABLET, FILM COATED in 1 BOTTLE (68788-7900-3)
  • 60 TABLET, FILM COATED in 1 BOTTLE (68788-7900-6)
  • 90 TABLET, FILM COATED in 1 BOTTLE (68788-7900-9)
source: ndc

Packages (4)

68788-7900-1 100 TABLET, FILM COATED in 1 BOTTLE (68788-7900-1) 68788-7900-3 30 TABLET, FILM COATED in 1 BOTTLE (68788-7900-3) 68788-7900-6 60 TABLET, FILM COATED in 1 BOTTLE (68788-7900-6) 68788-7900-9 90 TABLET, FILM COATED in 1 BOTTLE (68788-7900-9)

Ingredients (1)

ATORVASTATIN CALCIUM TRIHYDRATE (10 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": "d7038238-24d7-498e-988a-0448f095eb8d", "openfda": {"unii": ["48A5M73Z4Q"], "rxcui": ["617312"], "spl_set_id": ["7fc504dd-718a-4340-825f-e19ed76b71ef"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (68788-7900-1)", "package_ndc": "68788-7900-1", "marketing_start_date": "20210514"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68788-7900-3)", "package_ndc": "68788-7900-3", "marketing_start_date": "20210514"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (68788-7900-6)", "package_ndc": "68788-7900-6", "marketing_start_date": "20210514"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68788-7900-9)", "package_ndc": "68788-7900-9", "marketing_start_date": "20210514"}], "brand_name": "Atorvastatin Calcium", "product_id": "68788-7900_d7038238-24d7-498e-988a-0448f095eb8d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "68788-7900", "generic_name": "Atorvastatin Calcium", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Atorvastatin Calcium", "active_ingredients": [{"name": "ATORVASTATIN CALCIUM TRIHYDRATE", "strength": "10 mg/1"}], "application_number": "ANDA209288", "marketing_category": "ANDA", "marketing_start_date": "20210514", "listing_expiration_date": "20261231"}