Package 70518-2505-0

Brand: pravastatin sodium

Generic: pravastatin sodium
NDC Package

Package Facts

Identity

Package NDC 70518-2505-0
Digits Only 7051825050
Product NDC 70518-2505
Product ID 70518-2505_4a2c874e-7fc0-212b-e063-6294a90a7b66
Description

30 TABLET in 1 BLISTER PACK (70518-2505-0)

Marketing

Marketing Status
Discontinued 2026-09-30
Brand pravastatin sodium
Generic pravastatin sodium
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4a2c874e-7fc0-212b-e063-6294a90a7b66", "openfda": {"unii": ["3M8608UQ61"], "rxcui": ["904475"], "spl_set_id": ["7e400611-7432-4911-8662-1f0a740f76bb"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-2505-0)", "package_ndc": "70518-2505-0", "marketing_end_date": "20260930", "marketing_start_date": "20191224"}], "brand_name": "Pravastatin Sodium", "product_id": "70518-2505_4a2c874e-7fc0-212b-e063-6294a90a7b66", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "70518-2505", "generic_name": "Pravastatin Sodium", "labeler_name": "REMEDYREPACK 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": "20191224"}