Package 50090-7813-0

Brand: pravastatin sodium

Generic: pravastatin sodium
NDC Package

Package Facts

Identity

Package NDC 50090-7813-0
Digits Only 5009078130
Product NDC 50090-7813
Product ID 50090-7813_37270f57-2466-4585-9d18-6066a55bf121
Description

90 TABLET in 1 BOTTLE (50090-7813-0)

Marketing

Marketing Status
Marketed Since 2025-12-08
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": "37270f57-2466-4585-9d18-6066a55bf121", "openfda": {"unii": ["3M8608UQ61"], "rxcui": ["904467"], "spl_set_id": ["fd76794d-de33-4886-875c-fa05b2639f84"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-7813-0)", "package_ndc": "50090-7813-0", "marketing_start_date": "20251208"}], "brand_name": "PRAVASTATIN SODIUM", "product_id": "50090-7813_37270f57-2466-4585-9d18-6066a55bf121", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "50090-7813", "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": "ANDA076341", "marketing_category": "ANDA", "marketing_start_date": "20110718", "listing_expiration_date": "20261231"}