Package 50090-6970-0

Brand: atorvastatin calcium

Generic: atorvastatin calcium
NDC Package

Package Facts

Identity

Package NDC 50090-6970-0
Digits Only 5009069700
Product NDC 50090-6970
Description

90 TABLET, FILM COATED in 1 BOTTLE (50090-6970-0)

Marketing

Marketing Status
Marketed Since 2023-12-21
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": "ef01482a-e886-4594-9ae7-86fe08c43c5b", "openfda": {"unii": ["48A5M73Z4Q"], "rxcui": ["259255"], "spl_set_id": ["498ef8e6-3366-42f4-99fe-b3e1dedae887"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-6970-0)", "package_ndc": "50090-6970-0", "marketing_start_date": "20231221"}], "brand_name": "Atorvastatin calcium", "product_id": "50090-6970_ef01482a-e886-4594-9ae7-86fe08c43c5b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "50090-6970", "generic_name": "Atorvastatin calcium", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Atorvastatin calcium", "active_ingredients": [{"name": "ATORVASTATIN CALCIUM TRIHYDRATE", "strength": "80 mg/1"}], "application_number": "ANDA211933", "marketing_category": "ANDA", "marketing_start_date": "20190208", "listing_expiration_date": "20261231"}