Package 71335-2298-1

Brand: pravastatin sodium

Generic: pravastatin sodium
NDC Package

Package Facts

Identity

Package NDC 71335-2298-1
Digits Only 7133522981
Product NDC 71335-2298
Description

1000 TABLET in 1 BOTTLE (71335-2298-1)

Marketing

Marketing Status
Marketed Since 2023-12-01
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": "350cfca7-2d28-84c4-e063-6294a90af068", "openfda": {"unii": ["3M8608UQ61"], "rxcui": ["904458"], "spl_set_id": ["a7f75948-2958-44c8-b52f-5e39e80cdd1f"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (71335-2298-1)", "package_ndc": "71335-2298-1", "marketing_start_date": "20231201"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (71335-2298-2)", "package_ndc": "71335-2298-2", "marketing_start_date": "20231201"}], "brand_name": "PRAVASTATIN SODIUM", "product_id": "71335-2298_350cfca7-2d28-84c4-e063-6294a90af068", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "71335-2298", "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"}