Package 0093-7202-98

Brand: pravastatin sodium

Generic: pravastatin sodium
NDC Package

Package Facts

Identity

Package NDC 0093-7202-98
Digits Only 0093720298
Product NDC 0093-7202
Product ID 0093-7202_72579e23-23ef-4ab7-ad64-24d5ea7997eb
Description

90 TABLET in 1 BOTTLE (0093-7202-98)

Marketing

Marketing Status
Discontinued 2026-09-30
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": "72579e23-23ef-4ab7-ad64-24d5ea7997eb", "openfda": {"upc": ["0300937202981"], "unii": ["3M8608UQ61"], "rxcui": ["904458", "904467", "904475"], "spl_set_id": ["99e0e848-f8f3-4b42-b880-8fbc42633948"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (0093-7202-10)", "package_ndc": "0093-7202-10", "marketing_end_date": "20260930", "marketing_start_date": "20060425"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (0093-7202-98)", "package_ndc": "0093-7202-98", "marketing_end_date": "20260930", "marketing_start_date": "20060425"}], "brand_name": "Pravastatin Sodium", "product_id": "0093-7202_72579e23-23ef-4ab7-ad64-24d5ea7997eb", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "0093-7202", "generic_name": "Pravastatin Sodium", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pravastatin Sodium", "active_ingredients": [{"name": "PRAVASTATIN SODIUM", "strength": "40 mg/1"}], "application_number": "ANDA076056", "marketing_category": "ANDA", "marketing_end_date": "20260930", "marketing_start_date": "20060425"}