Package 67046-1621-3

Brand: pravastatin sodium

Generic: pravastatin sodium
NDC Package

Package Facts

Identity

Package NDC 67046-1621-3
Digits Only 6704616213
Product NDC 67046-1621
Description

30 TABLET in 1 BLISTER PACK (67046-1621-3)

Marketing

Marketing Status
Marketed Since 2025-12-08
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": "4573c662-e92e-dffe-e063-6294a90a71da", "openfda": {"unii": ["3M8608UQ61"], "rxcui": ["904458"], "spl_set_id": ["4573c42b-6d4a-e001-e063-6294a90acea1"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (67046-1621-3)", "package_ndc": "67046-1621-3", "marketing_start_date": "20251208"}], "brand_name": "PRAVASTATIN SODIUM", "product_id": "67046-1621_4573c662-e92e-dffe-e063-6294a90a71da", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "67046-1621", "generic_name": "PRAVASTATIN SODIUM", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PRAVASTATIN SODIUM", "active_ingredients": [{"name": "PRAVASTATIN SODIUM", "strength": "10 mg/1"}], "application_number": "ANDA076341", "marketing_category": "ANDA", "marketing_start_date": "20251208", "listing_expiration_date": "20261231"}