Package 72162-1951-0
Brand: pravastatin sodium
Generic: pravastatin sodiumPackage 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
Brand
pravastatin sodium
Generic
pravastatin sodium
Sample Package
No
Linked Drug Pages (1)
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"}