Package 82868-081-30

Brand: pravastatin sodium

Generic: pravastatin sodium
NDC Package

Package Facts

Identity

Package NDC 82868-081-30
Digits Only 8286808130
Product NDC 82868-081
Product ID 82868-081_472074f5-7926-aa3d-e063-6394a90a011a
Description

30 TABLET in 1 BOTTLE, PLASTIC (82868-081-30)

Marketing

Marketing Status
Marketed Since 2025-06-19
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": "472074f5-7926-aa3d-e063-6394a90a011a", "openfda": {"unii": ["3M8608UQ61"], "rxcui": ["904475"], "spl_set_id": ["47207487-0c6d-8da3-e063-6294a90a8aee"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (82868-081-30)", "package_ndc": "82868-081-30", "marketing_start_date": "20250619"}], "brand_name": "Pravastatin sodium", "product_id": "82868-081_472074f5-7926-aa3d-e063-6394a90a011a", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "82868-081", "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": "40 mg/1"}], "application_number": "ANDA209869", "marketing_category": "ANDA", "marketing_start_date": "20250619", "listing_expiration_date": "20261231"}