Package 82868-096-30

Brand: pravastatin sodium

Generic: pravastatin sodium
NDC Package

Package Facts

Identity

Package NDC 82868-096-30
Digits Only 8286809630
Product NDC 82868-096
Description

30 TABLET in 1 BOTTLE, PLASTIC (82868-096-30)

Marketing

Marketing Status
Marketed Since 2025-12-19
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": "471b4a51-f08f-52a6-e063-6294a90a32d9", "openfda": {"unii": ["3M8608UQ61"], "rxcui": ["904475"], "spl_set_id": ["471b4dac-057d-740c-e063-6294a90af9e9"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (82868-096-30)", "package_ndc": "82868-096-30", "marketing_start_date": "20251219"}], "brand_name": "Pravastatin sodium", "product_id": "82868-096_471b4a51-f08f-52a6-e063-6294a90a32d9", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "82868-096", "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": "ANDA076056", "marketing_category": "ANDA", "marketing_start_date": "20251219", "listing_expiration_date": "20261231"}