Package 70518-4339-0

Brand: pravastatin sodium

Generic: pravastatin sodium
NDC Package

Package Facts

Identity

Package NDC 70518-4339-0
Digits Only 7051843390
Product NDC 70518-4339
Description

30 TABLET in 1 BLISTER PACK (70518-4339-0)

Marketing

Marketing Status
Marketed Since 2025-05-13
Brand pravastatin sodium
Generic pravastatin sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4030e199-7260-81fc-e063-6394a90a315b", "openfda": {"unii": ["3M8608UQ61"], "rxcui": ["904475"], "spl_set_id": ["fa152ce7-6c07-4aaf-9374-932ce81d0cf9"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-4339-0)", "package_ndc": "70518-4339-0", "marketing_start_date": "20250513"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (70518-4339-1)", "package_ndc": "70518-4339-1", "marketing_start_date": "20250825"}], "brand_name": "Pravastatin sodium", "product_id": "70518-4339_4030e199-7260-81fc-e063-6394a90a315b", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "70518-4339", "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_start_date": "20250513", "listing_expiration_date": "20261231"}