Package 72189-239-90

Brand: atorvastatin calcium

Generic: atorvastatin calcium
NDC Package

Package Facts

Identity

Package NDC 72189-239-90
Digits Only 7218923990
Product NDC 72189-239
Product ID 72189-239_2c283f9f-1dbb-4a4c-e063-6394a90a7953
Description

90 TABLET in 1 BOTTLE (72189-239-90)

Marketing

Marketing Status
Marketed Since 2021-09-20
Brand atorvastatin calcium
Generic atorvastatin calcium
Sample Package No

Linked Drug Pages (1)

ATORVASTATIN CALCIUM ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2c283f9f-1dbb-4a4c-e063-6394a90a7953", "openfda": {"unii": ["48A5M73Z4Q"], "rxcui": ["617312"], "spl_set_id": ["c3b70f79-45a3-0869-e053-2a95a90a3cdb"], "manufacturer_name": ["DIRECT RX"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (72189-239-90)", "package_ndc": "72189-239-90", "marketing_start_date": "20210920"}], "brand_name": "ATORVASTATIN CALCIUM", "product_id": "72189-239_2c283f9f-1dbb-4a4c-e063-6394a90a7953", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "72189-239", "generic_name": "ATORVASTATIN CALCIUM", "labeler_name": "DIRECT RX", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ATORVASTATIN CALCIUM", "active_ingredients": [{"name": "ATORVASTATIN CALCIUM TRIHYDRATE", "strength": "40 mg/1"}], "application_number": "ANDA204991", "marketing_category": "ANDA", "marketing_start_date": "20210920", "listing_expiration_date": "20261231"}