Package 50090-7709-0

Brand: pravastatin sodium

Generic: pravastatin sodium
NDC Package

Package Facts

Identity

Package NDC 50090-7709-0
Digits Only 5009077090
Product NDC 50090-7709
Description

30 TABLET in 1 BOTTLE (50090-7709-0)

Marketing

Marketing Status
Marketed Since 2025-10-14
Brand pravastatin sodium
Generic pravastatin sodium
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f0d2cf93-5c22-4df7-b66a-0b90ce2a614b", "openfda": {"unii": ["3M8608UQ61"], "rxcui": ["904467"], "spl_set_id": ["635062df-9a84-4ff8-874c-dcee581a5555"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-7709-0)", "package_ndc": "50090-7709-0", "marketing_start_date": "20251014"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-7709-1)", "package_ndc": "50090-7709-1", "marketing_start_date": "20251014"}], "brand_name": "PRAVASTATIN SODIUM", "product_id": "50090-7709_f0d2cf93-5c22-4df7-b66a-0b90ce2a614b", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "50090-7709", "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": "20240601", "listing_expiration_date": "20261231"}