Package 51655-070-52

Brand: pravastatin sodium

Generic: pravastatin sodium
NDC Package

Package Facts

Identity

Package NDC 51655-070-52
Digits Only 5165507052
Product NDC 51655-070
Product ID 51655-070_46ddc2ac-c492-4747-e063-6294a90a8c56
Description

30 TABLET in 1 BOTTLE, PLASTIC (51655-070-52)

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": "46ddc2ac-c492-4747-e063-6294a90a8c56", "openfda": {"unii": ["3M8608UQ61"], "rxcui": ["904458"], "spl_set_id": ["f2a18ecb-07db-e54d-e053-2995a90a8745"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (51655-070-52)", "package_ndc": "51655-070-52", "marketing_end_date": "20260331", "marketing_start_date": "20220928"}], "brand_name": "Pravastatin Sodium", "product_id": "51655-070_46ddc2ac-c492-4747-e063-6294a90a8c56", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "51655-070", "generic_name": "Pravastatin Sodium", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pravastatin Sodium", "active_ingredients": [{"name": "PRAVASTATIN SODIUM", "strength": "10 mg/1"}], "application_number": "ANDA076056", "marketing_category": "ANDA", "marketing_end_date": "20260331", "marketing_start_date": "20220928"}