atorvastatin calcium

Generic: atorvastatin calcium

Labeler: dr. reddy's laboratories limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name atorvastatin calcium
Generic Name atorvastatin calcium
Labeler dr. reddy's laboratories limited
Dosage Form TABLET
Routes
ORAL
Active Ingredients

atorvastatin calcium trihydrate 40 mg/1

Manufacturer
Dr. Reddy's Laboratories Limited

Identifiers & Regulatory

Product NDC 55111-123
Product ID 55111-123_36e09eff-3948-2638-b633-d5ec2bc03d2a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA091650
Listing Expiration 2026-12-31
Marketing Start 2012-07-17

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 55111123
Hyphenated Format 55111-123

Supplemental Identifiers

RxCUI
617310 617311 617312
UPC
0355111123903
UNII
48A5M73Z4Q

Packaging Origin

Original Packager
true

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 ANDA091650 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 500 TABLET in 1 BOTTLE (55111-123-05)
  • 1000 TABLET in 1 BOTTLE (55111-123-10)
  • 30 TABLET in 1 BOTTLE (55111-123-30)
  • 60 TABLET in 1 BOTTLE (55111-123-60)
  • 90 TABLET in 1 BOTTLE (55111-123-90)
source: ndc

Packages (5)

55111-123-05 500 TABLET in 1 BOTTLE (55111-123-05) 55111-123-10 1000 TABLET in 1 BOTTLE (55111-123-10) 55111-123-30 30 TABLET in 1 BOTTLE (55111-123-30) 55111-123-60 60 TABLET in 1 BOTTLE (55111-123-60) 55111-123-90 90 TABLET in 1 BOTTLE (55111-123-90)

Ingredients (1)

atorvastatin calcium trihydrate (40 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": "36e09eff-3948-2638-b633-d5ec2bc03d2a", "openfda": {"upc": ["0355111123903"], "unii": ["48A5M73Z4Q"], "rxcui": ["617310", "617311", "617312"], "spl_set_id": ["901550e6-22be-68c9-eb86-f85a9c9dd998"], "manufacturer_name": ["Dr. Reddy's Laboratories Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (55111-123-05)", "package_ndc": "55111-123-05", "marketing_start_date": "20120717"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (55111-123-10)", "package_ndc": "55111-123-10", "marketing_start_date": "20120717"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (55111-123-30)", "package_ndc": "55111-123-30", "marketing_start_date": "20120717"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (55111-123-60)", "package_ndc": "55111-123-60", "marketing_start_date": "20120717"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (55111-123-90)", "package_ndc": "55111-123-90", "marketing_start_date": "20120717"}], "brand_name": "Atorvastatin Calcium", "product_id": "55111-123_36e09eff-3948-2638-b633-d5ec2bc03d2a", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "55111-123", "generic_name": "Atorvastatin Calcium", "labeler_name": "Dr. Reddy's Laboratories Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Atorvastatin Calcium", "active_ingredients": [{"name": "ATORVASTATIN CALCIUM TRIHYDRATE", "strength": "40 mg/1"}], "application_number": "ANDA091650", "marketing_category": "ANDA", "marketing_start_date": "20120717", "listing_expiration_date": "20261231"}