Package 72162-1951-0

Brand: pravastatin sodium

Generic: pravastatin sodium
NDC Package

Package Facts

Identity

Package NDC 72162-1951-0
Digits Only 7216219510
Product NDC 72162-1951
Description

1000 TABLET in 1 BOTTLE (72162-1951-0)

Marketing

Marketing Status
Marketed Since 2023-10-25
Brand pravastatin sodium
Generic pravastatin sodium
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "640ea028-2f8d-43c6-bb98-71ef8b955883", "openfda": {"unii": ["3M8608UQ61"], "rxcui": ["904458"], "spl_set_id": ["7b7f5c28-78fa-4625-ad69-4291500e033d"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (72162-1951-0)", "package_ndc": "72162-1951-0", "marketing_start_date": "20231025"}], "brand_name": "PRAVASTATIN SODIUM", "product_id": "72162-1951_640ea028-2f8d-43c6-bb98-71ef8b955883", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "72162-1951", "generic_name": "PRAVASTATIN SODIUM", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PRAVASTATIN SODIUM", "active_ingredients": [{"name": "PRAVASTATIN SODIUM", "strength": "10 mg/1"}], "application_number": "ANDA209869", "marketing_category": "ANDA", "marketing_start_date": "20210201", "listing_expiration_date": "20261231"}