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
Routes
ORAL
Active Ingredients

ATORVASTATIN 10 mg/1

Identifiers & Regulatory

Product NDC 68788-8656
Product ID 68788-8656_1237b2c6-eecd-4a5a-8ac5-80affabef7f0
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA213853
Listing Expiration 2026-12-31
Marketing Start 2024-05-09

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 687888656
Hyphenated Format 68788-8656

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 ANDA213853 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 36 TABLET in 1 BOTTLE (68788-8656-3)
  • 60 TABLET in 1 BOTTLE (68788-8656-6)
  • 90 TABLET in 1 BOTTLE (68788-8656-9)
source: ndc

Packages (3)

68788-8656-3 36 TABLET in 1 BOTTLE (68788-8656-3) 68788-8656-6 60 TABLET in 1 BOTTLE (68788-8656-6) 68788-8656-9 90 TABLET in 1 BOTTLE (68788-8656-9)

Ingredients (1)

ATORVASTATIN (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": "1237b2c6-eecd-4a5a-8ac5-80affabef7f0", "openfda": {"nui": ["N0000175589", "N0000000121"], "unii": ["A0JWA85V8F"], "rxcui": ["617312"], "spl_set_id": ["d781f16d-6964-48c3-8361-17174d1aa969"], "pharm_class_epc": ["HMG-CoA Reductase Inhibitor [EPC]"], "pharm_class_moa": ["Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "36 TABLET in 1 BOTTLE (68788-8656-3)", "package_ndc": "68788-8656-3", "marketing_start_date": "20240509"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68788-8656-6)", "package_ndc": "68788-8656-6", "marketing_start_date": "20240509"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68788-8656-9)", "package_ndc": "68788-8656-9", "marketing_start_date": "20240509"}], "brand_name": "Atorvastatin calcium", "product_id": "68788-8656_1237b2c6-eecd-4a5a-8ac5-80affabef7f0", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "68788-8656", "generic_name": "Atorvastatin calcium", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Atorvastatin calcium", "active_ingredients": [{"name": "ATORVASTATIN", "strength": "10 mg/1"}], "application_number": "ANDA213853", "marketing_category": "ANDA", "marketing_start_date": "20240509", "listing_expiration_date": "20261231"}