Package 70518-3304-1

Brand: atorvastatin calcium

Generic: atorvastatin calcium
NDC Package

Package Facts

Identity

Package NDC 70518-3304-1
Digits Only 7051833041
Product NDC 70518-3304
Product ID 70518-3304_3a7222e4-4883-cb5c-e063-6394a90ab6cb
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3304-1)

Marketing

Marketing Status
Marketed Since 2022-12-06
Brand atorvastatin calcium
Generic atorvastatin calcium
Sample Package No

Linked Drug Pages (1)

Atorvastatin calcium ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3a7222e4-4883-cb5c-e063-6394a90ab6cb", "openfda": {"unii": ["48A5M73Z4Q"], "rxcui": ["259255"], "spl_set_id": ["51e24220-3374-4e5e-9a8d-4113002c5bed"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3304-1)", "package_ndc": "70518-3304-1", "marketing_start_date": "20221206"}], "brand_name": "Atorvastatin calcium", "product_id": "70518-3304_3a7222e4-4883-cb5c-e063-6394a90ab6cb", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "70518-3304", "generic_name": "Atorvastatin calcium", "labeler_name": "REMEDYREPACK INC.", "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": "20211222", "listing_expiration_date": "20261231"}