Package 0093-7446-01

Brand: fluvastatin sodium

Generic: fluvastatin sodium
NDC Package

Package Facts

Identity

Package NDC 0093-7446-01
Digits Only 0093744601
Product NDC 0093-7446
Description

100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0093-7446-01)

Marketing

Marketing Status
Marketed Since 2016-06-02
Brand fluvastatin sodium
Generic fluvastatin sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "82469f87-7755-4dda-a92d-a27856d0fe0e", "openfda": {"upc": ["0300937446019"], "unii": ["PYF7O1FV7F"], "rxcui": ["360507"], "spl_set_id": ["cc55110f-1ad6-4f97-840d-62b3a5ac415a"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0093-7446-01)", "package_ndc": "0093-7446-01", "marketing_start_date": "20160602"}, {"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0093-7446-56)", "package_ndc": "0093-7446-56", "marketing_start_date": "20160602"}], "brand_name": "Fluvastatin Sodium", "product_id": "0093-7446_82469f87-7755-4dda-a92d-a27856d0fe0e", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "0093-7446", "generic_name": "Fluvastatin Sodium", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluvastatin Sodium", "active_ingredients": [{"name": "FLUVASTATIN SODIUM", "strength": "80 mg/1"}], "application_number": "ANDA079011", "marketing_category": "ANDA", "marketing_start_date": "20160602", "listing_expiration_date": "20261231"}