Package 68071-3667-3

Brand: atorvastatin calcium

Generic: atorvastatin calcium
NDC Package

Package Facts

Identity

Package NDC 68071-3667-3
Digits Only 6807136673
Product NDC 68071-3667
Description

30 TABLET, FILM COATED in 1 BOTTLE (68071-3667-3)

Marketing

Marketing Status
Marketed Since 2024-08-19
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": "4c4af2a4-99f6-44cd-e063-6294a90a58aa", "openfda": {"upc": ["0368071366730"], "unii": ["48A5M73Z4Q"], "rxcui": ["617311"], "spl_set_id": ["200c1994-9327-e02c-e063-6394a90a593d"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68071-3667-3)", "package_ndc": "68071-3667-3", "marketing_start_date": "20240819"}], "brand_name": "ATORVASTATIN CALCIUM", "product_id": "68071-3667_4c4af2a4-99f6-44cd-e063-6294a90a58aa", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "68071-3667", "generic_name": "ATORVASTATIN CALCIUM", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ATORVASTATIN CALCIUM", "active_ingredients": [{"name": "ATORVASTATIN CALCIUM TRIHYDRATE", "strength": "40 mg/1"}], "application_number": "ANDA214344", "marketing_category": "ANDA", "marketing_start_date": "20230912", "listing_expiration_date": "20271231"}