Package 67046-1519-3

Brand: pravastatin sodium

Generic: pravastatin sodium
NDC Package

Package Facts

Identity

Package NDC 67046-1519-3
Digits Only 6704615193
Product NDC 67046-1519
Description

30 TABLET in 1 BLISTER PACK (67046-1519-3)

Marketing

Marketing Status
Marketed Since 2025-02-13
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": "2e07a4ba-25fe-a248-e063-6294a90abb0b", "openfda": {"unii": ["3M8608UQ61"], "rxcui": ["904467"], "spl_set_id": ["2e07ad78-1059-e0ec-e063-6394a90a9bff"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (67046-1519-3)", "package_ndc": "67046-1519-3", "marketing_start_date": "20250213"}], "brand_name": "PRAVASTATIN SODIUM", "product_id": "67046-1519_2e07a4ba-25fe-a248-e063-6294a90abb0b", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "67046-1519", "generic_name": "PRAVASTATIN SODIUM", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PRAVASTATIN SODIUM", "active_ingredients": [{"name": "PRAVASTATIN SODIUM", "strength": "20 mg/1"}], "application_number": "ANDA077987", "marketing_category": "ANDA", "marketing_start_date": "20250213", "listing_expiration_date": "20261231"}