Package 0781-8017-31

Brand: fluvastatin sodium er

Generic: fluvastatin sodium
NDC Package

Package Facts

Identity

Package NDC 0781-8017-31
Digits Only 0781801731
Product NDC 0781-8017
Description

30 TABLET, EXTENDED RELEASE in 1 BOTTLE (0781-8017-31)

Marketing

Marketing Status
Marketed Since 2018-05-02
Brand fluvastatin sodium er
Generic fluvastatin sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "37375ca6-3a81-4d10-9b39-9aee948e51a4", "openfda": {"upc": ["0307818017313"], "unii": ["PYF7O1FV7F"], "rxcui": ["360507"], "spl_set_id": ["5ab4296c-87c2-4c64-b218-d620eef51310"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0781-8017-01)", "package_ndc": "0781-8017-01", "marketing_start_date": "20180502"}, {"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (0781-8017-31)", "package_ndc": "0781-8017-31", "marketing_start_date": "20180502"}], "brand_name": "FLUVASTATIN SODIUM ER", "product_id": "0781-8017_37375ca6-3a81-4d10-9b39-9aee948e51a4", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "0781-8017", "generic_name": "fluvastatin sodium", "labeler_name": "Sandoz Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "FLUVASTATIN SODIUM", "brand_name_suffix": "ER", "active_ingredients": [{"name": "FLUVASTATIN SODIUM", "strength": "80 mg/1"}], "application_number": "NDA021192", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20151016", "listing_expiration_date": "20261231"}