Package 50090-7551-1

Brand: pravastatin sodium

Generic: pravastatin sodium
NDC Package

Package Facts

Identity

Package NDC 50090-7551-1
Digits Only 5009075511
Product NDC 50090-7551
Description

90 TABLET in 1 BOTTLE (50090-7551-1)

Marketing

Marketing Status
Marketed Since 2025-05-23
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": "a147a04b-630a-4280-9663-fef59cc8fef0", "openfda": {"unii": ["3M8608UQ61"], "rxcui": ["904467"], "spl_set_id": ["b7a84cc1-f6e4-40be-9e68-cf7d43bbd617"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-7551-0)", "package_ndc": "50090-7551-0", "marketing_start_date": "20250523"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-7551-1)", "package_ndc": "50090-7551-1", "marketing_start_date": "20250523"}], "brand_name": "Pravastatin Sodium", "product_id": "50090-7551_a147a04b-630a-4280-9663-fef59cc8fef0", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "50090-7551", "generic_name": "Pravastatin Sodium", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pravastatin Sodium", "active_ingredients": [{"name": "PRAVASTATIN SODIUM", "strength": "20 mg/1"}], "application_number": "ANDA077987", "marketing_category": "ANDA", "marketing_start_date": "20220812", "listing_expiration_date": "20261231"}