Package 71335-2848-1

Brand: pravastatin sodium

Generic: pravastatin sodium
NDC Package

Package Facts

Identity

Package NDC 71335-2848-1
Digits Only 7133528481
Product NDC 71335-2848
Description

90 TABLET in 1 BOTTLE (71335-2848-1)

Marketing

Marketing Status
Marketed Since 2025-11-10
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": "34873359-fe19-4061-9912-c35509f9f9ed", "openfda": {"unii": ["3M8608UQ61"], "rxcui": ["904458"], "spl_set_id": ["4ed7a4d1-1183-4d95-8311-6d3e58feafa8"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-2848-1)", "package_ndc": "71335-2848-1", "marketing_start_date": "20251110"}], "brand_name": "Pravastatin sodium", "product_id": "71335-2848_34873359-fe19-4061-9912-c35509f9f9ed", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "71335-2848", "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"}