atorvastatin calcium

Generic: atorvastatin calcium, film coated

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name atorvastatin calcium
Generic Name atorvastatin calcium, film coated
Labeler proficient rx lp
Dosage Form TABLET
Routes
ORAL
Active Ingredients

atorvastatin calcium trihydrate 10 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-802
Product ID 71205-802_cd756dc8-6c30-4273-8947-9a3f9b4fc075
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209912
Listing Expiration 2026-12-31
Marketing Start 2018-06-18

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 71205802
Hyphenated Format 71205-802

Supplemental Identifiers

RxCUI
617312
UPC
0371205802905
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, film coated (source: ndc)
Application Number ANDA209912 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (71205-802-30)
  • 60 TABLET in 1 BOTTLE (71205-802-60)
  • 90 TABLET in 1 BOTTLE (71205-802-90)
source: ndc

Packages (3)

71205-802-30 30 TABLET in 1 BOTTLE (71205-802-30) 71205-802-60 60 TABLET in 1 BOTTLE (71205-802-60) 71205-802-90 90 TABLET in 1 BOTTLE (71205-802-90)

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": "cd756dc8-6c30-4273-8947-9a3f9b4fc075", "openfda": {"upc": ["0371205802905"], "unii": ["48A5M73Z4Q"], "rxcui": ["617312"], "spl_set_id": ["cd756dc8-6c30-4273-8947-9a3f9b4fc075"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71205-802-30)", "package_ndc": "71205-802-30", "marketing_start_date": "20230518"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71205-802-60)", "package_ndc": "71205-802-60", "marketing_start_date": "20230518"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71205-802-90)", "package_ndc": "71205-802-90", "marketing_start_date": "20230518"}], "brand_name": "atorvastatin calcium", "product_id": "71205-802_cd756dc8-6c30-4273-8947-9a3f9b4fc075", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "71205-802", "generic_name": "atorvastatin calcium, film coated", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "atorvastatin calcium", "active_ingredients": [{"name": "ATORVASTATIN CALCIUM TRIHYDRATE", "strength": "10 mg/1"}], "application_number": "ANDA209912", "marketing_category": "ANDA", "marketing_start_date": "20180618", "listing_expiration_date": "20261231"}