Package 51655-881-30

Brand: atorvastatin calcium

Generic: atorvastatin calcium
NDC Package

Package Facts

Identity

Package NDC 51655-881-30
Digits Only 5165588130
Product NDC 51655-881
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-881-30)

Marketing

Marketing Status
Marketed Since 2022-07-07
Brand atorvastatin calcium
Generic atorvastatin calcium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4973fd67-4cd2-1b98-e063-6394a90a103b", "openfda": {"unii": ["YRZ789OWMI"], "rxcui": ["259255"], "spl_set_id": ["f76b9e48-3ef7-e15a-e053-6394a90aed58"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-881-30)", "package_ndc": "51655-881-30", "marketing_start_date": "20220707"}], "brand_name": "ATORVASTATIN CALCIUM", "product_id": "51655-881_4973fd67-4cd2-1b98-e063-6394a90a103b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "51655-881", "generic_name": "ATORVASTATIN CALCIUM", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ATORVASTATIN CALCIUM", "active_ingredients": [{"name": "ATORVASTATIN CALCIUM PROPYLENE GLYCOL SOLVATE", "strength": "80 mg/1"}], "application_number": "ANDA090548", "marketing_category": "ANDA", "marketing_start_date": "20220707", "listing_expiration_date": "20271231"}