Package 68071-3868-3

Brand: atorvastatin calcium

Generic: atorvastatin calcium, film coated
NDC Package

Package Facts

Identity

Package NDC 68071-3868-3
Digits Only 6807138683
Product NDC 68071-3868
Description

30 TABLET in 1 BOTTLE (68071-3868-3)

Marketing

Marketing Status
Marketed Since 2025-06-13
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": "37780cb8-06f8-2263-e063-6394a90abba8", "openfda": {"upc": ["0368071386837"], "unii": ["48A5M73Z4Q"], "rxcui": ["617312"], "spl_set_id": ["3778125d-b3d9-2853-e063-6394a90aa863"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68071-3868-3)", "package_ndc": "68071-3868-3", "marketing_start_date": "20250613"}], "brand_name": "Atorvastatin Calcium", "product_id": "68071-3868_37780cb8-06f8-2263-e063-6394a90abba8", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "68071-3868", "generic_name": "atorvastatin calcium, film coated", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Atorvastatin Calcium", "active_ingredients": [{"name": "ATORVASTATIN CALCIUM TRIHYDRATE", "strength": "10 mg/1"}], "application_number": "ANDA209912", "marketing_category": "ANDA", "marketing_start_date": "20231020", "listing_expiration_date": "20261231"}