Package 16571-139-10

Brand: atorvastatin calcium

Generic: atorvastatin calcium, film coated
NDC Package

Package Facts

Identity

Package NDC 16571-139-10
Digits Only 1657113910
Product NDC 16571-139
Description

1000 TABLET in 1 BOTTLE (16571-139-10)

Marketing

Marketing Status
Marketed Since 2023-10-20
Brand atorvastatin calcium
Generic atorvastatin calcium, film coated
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "b94c6347-161c-44f2-8937-34c5098bf755", "openfda": {"upc": ["0316571136094", "0316571138098", "0316571137091"], "unii": ["48A5M73Z4Q"], "rxcui": ["259255", "617310", "617311", "617312"], "spl_set_id": ["73cefb0b-1747-4fe0-b252-377f4ed94c6f"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (16571-139-09)", "package_ndc": "16571-139-09", "marketing_start_date": "20231020"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (16571-139-10)", "package_ndc": "16571-139-10", "marketing_start_date": "20231020"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (16571-139-50)", "package_ndc": "16571-139-50", "marketing_start_date": "20231020"}], "brand_name": "Atorvastatin Calcium", "product_id": "16571-139_b94c6347-161c-44f2-8937-34c5098bf755", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "16571-139", "generic_name": "atorvastatin calcium, film coated", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Atorvastatin Calcium", "active_ingredients": [{"name": "ATORVASTATIN CALCIUM TRIHYDRATE", "strength": "80 mg/1"}], "application_number": "ANDA209912", "marketing_category": "ANDA", "marketing_start_date": "20231020", "listing_expiration_date": "20261231"}