Package 72162-1034-1

Brand: fluvastatin

Generic: fluvastatin
NDC Package

Package Facts

Identity

Package NDC 72162-1034-1
Digits Only 7216210341
Product NDC 72162-1034
Description

100 CAPSULE in 1 BOTTLE (72162-1034-1)

Marketing

Marketing Status
Marketed Since 2024-05-16
Brand fluvastatin
Generic fluvastatin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "b37d7bf2-b2f1-4843-b49b-1fde982a0f4a", "openfda": {"unii": ["PYF7O1FV7F"], "rxcui": ["310405"], "spl_set_id": ["ccd6bbe1-e293-4e1c-9ec4-e6c217612e77"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (72162-1034-1)", "package_ndc": "72162-1034-1", "marketing_start_date": "20240516"}], "brand_name": "Fluvastatin", "product_id": "72162-1034_b37d7bf2-b2f1-4843-b49b-1fde982a0f4a", "dosage_form": "CAPSULE", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "72162-1034", "generic_name": "Fluvastatin", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluvastatin", "active_ingredients": [{"name": "FLUVASTATIN SODIUM", "strength": "40 mg/1"}], "application_number": "ANDA078407", "marketing_category": "ANDA", "marketing_start_date": "20120705", "listing_expiration_date": "20261231"}