Package 67296-2130-9

Brand: atorvastatin calcium

Generic: atorvastatin calcium
NDC Package

Package Facts

Identity

Package NDC 67296-2130-9
Digits Only 6729621309
Product NDC 67296-2130
Description

90 TABLET, FILM COATED in 1 BOTTLE (67296-2130-9)

Marketing

Marketing Status
Marketed Since 2023-09-12
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": "46ac9d61-9c2b-7e4a-e063-6294a90a241f", "openfda": {"upc": ["0331722425902", "0331722427906", "0331722424905", "0331722426909"], "unii": ["48A5M73Z4Q"], "rxcui": ["617312"], "spl_set_id": ["301ef8f1-6b5f-234b-e063-6294a90ad2d3"], "manufacturer_name": ["Redpharm Drug"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (67296-2130-9)", "package_ndc": "67296-2130-9", "marketing_start_date": "20230912"}], "brand_name": "ATORVASTATIN CALCIUM", "product_id": "67296-2130_46ac9d61-9c2b-7e4a-e063-6294a90a241f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "67296-2130", "generic_name": "ATORVASTATIN CALCIUM", "labeler_name": "Redpharm Drug", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ATORVASTATIN CALCIUM", "active_ingredients": [{"name": "ATORVASTATIN CALCIUM TRIHYDRATE", "strength": "10 mg/1"}], "application_number": "ANDA214344", "marketing_category": "ANDA", "marketing_start_date": "20230912", "listing_expiration_date": "20261231"}