Package 50090-7552-0

Brand: pravastatin sodium

Generic: pravastatin sodium
NDC Package

Package Facts

Identity

Package NDC 50090-7552-0
Digits Only 5009075520
Product NDC 50090-7552
Product ID 50090-7552_214ec2bb-546f-4161-8bae-6317452e4abf
Description

90 TABLET in 1 BOTTLE (50090-7552-0)

Marketing

Marketing Status
Marketed Since 2025-05-23
Brand pravastatin sodium
Generic pravastatin sodium
Sample Package No

Linked Drug Pages (1)

Pravastatin Sodium ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "214ec2bb-546f-4161-8bae-6317452e4abf", "openfda": {"unii": ["3M8608UQ61"], "rxcui": ["904467"], "spl_set_id": ["4015f184-b57e-4d32-9cef-15c6e1cefe24"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-7552-0)", "package_ndc": "50090-7552-0", "marketing_start_date": "20250523"}], "brand_name": "Pravastatin Sodium", "product_id": "50090-7552_214ec2bb-546f-4161-8bae-6317452e4abf", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "50090-7552", "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"}