Package 35356-125-30

Brand: pravastatin sodium

Generic: pravastatin sodium
NDC Package

Package Facts

Identity

Package NDC 35356-125-30
Digits Only 3535612530
Product NDC 35356-125
Product ID 35356-125_77f23591-e677-43b5-8ed8-47059fc8ed3f
Description

30 TABLET in 1 BOTTLE (35356-125-30)

Marketing

Marketing Status
Discontinued 2026-03-31
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": "77f23591-e677-43b5-8ed8-47059fc8ed3f", "openfda": {"unii": ["3M8608UQ61"], "rxcui": ["904458", "904467", "904475"], "spl_set_id": ["e7194af1-6304-4e3e-88ab-0825706a3962"], "manufacturer_name": ["Lake Erie Medical DBA Quality Care Products LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (35356-125-30)", "package_ndc": "35356-125-30", "marketing_end_date": "20260331", "marketing_start_date": "20110718"}], "brand_name": "Pravastatin Sodium", "product_id": "35356-125_77f23591-e677-43b5-8ed8-47059fc8ed3f", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "35356-125", "generic_name": "pravastatin sodium", "labeler_name": "Lake Erie Medical DBA Quality Care Products LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pravastatin Sodium", "active_ingredients": [{"name": "PRAVASTATIN SODIUM", "strength": "40 mg/1"}], "application_number": "ANDA076341", "marketing_category": "ANDA", "marketing_end_date": "20260331", "marketing_start_date": "20110718"}