atorvastatin calcium
Generic: atorvastatin calcium
Labeler: remedyrepack inc.Drug Facts
Product Profile
Brand Name
atorvastatin calcium
Generic Name
atorvastatin calcium
Labeler
remedyrepack inc.
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
atorvastatin calcium trihydrate 20 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
70518-3037
Product ID
70518-3037_4ab4bba0-b4e9-19a9-e063-6294a90a9df5
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA209288
Listing Expiration
2027-12-31
Marketing Start
2021-03-03
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
705183037
Hyphenated Format
70518-3037
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
ANDA209288 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/1
Packaging
- 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3037-2)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4ab4bba0-b4e9-19a9-e063-6294a90a9df5", "openfda": {"unii": ["48A5M73Z4Q"], "rxcui": ["617310"], "spl_set_id": ["09cb8375-075c-47e8-a4eb-8ac667ed849e"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3037-2)", "package_ndc": "70518-3037-2", "marketing_start_date": "20250319"}], "brand_name": "Atorvastatin Calcium", "product_id": "70518-3037_4ab4bba0-b4e9-19a9-e063-6294a90a9df5", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "70518-3037", "generic_name": "Atorvastatin Calcium", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Atorvastatin Calcium", "active_ingredients": [{"name": "ATORVASTATIN CALCIUM TRIHYDRATE", "strength": "20 mg/1"}], "application_number": "ANDA209288", "marketing_category": "ANDA", "marketing_start_date": "20210303", "listing_expiration_date": "20271231"}