Package 70518-2887-1

Brand: pravastatin sodium

Generic: pravastatin sodium
NDC Package

Package Facts

Identity

Package NDC 70518-2887-1
Digits Only 7051828871
Product NDC 70518-2887
Product ID 70518-2887_4ab8510c-0de1-0008-e063-6394a90ab878
Description

90 TABLET in 1 BOTTLE, PLASTIC (70518-2887-1)

Marketing

Marketing Status
Discontinued 2026-08-31
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": "4ab8510c-0de1-0008-e063-6394a90ab878", "openfda": {"unii": ["3M8608UQ61"], "rxcui": ["904467"], "spl_set_id": ["0c4b59f1-92a8-44f8-8b4c-691f35777460"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (70518-2887-1)", "package_ndc": "70518-2887-1", "marketing_end_date": "20260831", "marketing_start_date": "20220916"}], "brand_name": "Pravastatin Sodium", "product_id": "70518-2887_4ab8510c-0de1-0008-e063-6394a90ab878", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "70518-2887", "generic_name": "Pravastatin Sodium", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pravastatin Sodium", "active_ingredients": [{"name": "PRAVASTATIN SODIUM", "strength": "20 mg/1"}], "application_number": "ANDA076056", "marketing_category": "ANDA", "marketing_end_date": "20260831", "marketing_start_date": "20200915"}