Package 68071-3470-6
Brand: atorvastatin calcium
Generic: atorvastatin film coatedPackage Facts
Identity
Package NDC
68071-3470-6
Digits Only
6807134706
Product NDC
68071-3470
Description
60 TABLET in 1 BOTTLE (68071-3470-6)
Marketing
Marketing Status
Brand
atorvastatin calcium
Generic
atorvastatin film coated
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "29299c94-9c96-b16e-e063-6394a90ac903", "openfda": {"upc": ["0368071347067"], "unii": ["48A5M73Z4Q"], "rxcui": ["617310"], "spl_set_id": ["01683314-5996-dbe4-e063-6394a90aa07a"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (68071-3470-6)", "package_ndc": "68071-3470-6", "marketing_start_date": "20230726"}], "brand_name": "atorvastatin calcium", "product_id": "68071-3470_29299c94-9c96-b16e-e063-6394a90ac903", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "68071-3470", "generic_name": "atorvastatin film coated", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "atorvastatin calcium", "active_ingredients": [{"name": "ATORVASTATIN CALCIUM TRIHYDRATE", "strength": "20 mg/1"}], "application_number": "ANDA209912", "marketing_category": "ANDA", "marketing_start_date": "20180618", "listing_expiration_date": "20261231"}