Package 84386-034-99

Brand: pravastatin sodium

Generic: pravastatin sodium
NDC Package

Package Facts

Identity

Package NDC 84386-034-99
Digits Only 8438603499
Product NDC 84386-034
Description

1000 TABLET in 1 BOTTLE (84386-034-99)

Marketing

Marketing Status
Marketed Since 2025-02-27
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": "c21d4797-d252-4073-891f-330484c5f643", "openfda": {"upc": ["0384386034904"], "unii": ["3M8608UQ61"], "rxcui": ["904481"], "spl_set_id": ["c21d4797-d252-4073-891f-330484c5f643"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (84386-034-90)", "package_ndc": "84386-034-90", "marketing_start_date": "20250227"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (84386-034-99)", "package_ndc": "84386-034-99", "marketing_start_date": "20250227"}], "brand_name": "Pravastatin sodium", "product_id": "84386-034_c21d4797-d252-4073-891f-330484c5f643", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "84386-034", "generic_name": "Pravastatin sodium", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pravastatin sodium", "active_ingredients": [{"name": "PRAVASTATIN SODIUM", "strength": "80 mg/1"}], "application_number": "ANDA077793", "marketing_category": "ANDA", "marketing_start_date": "20250227", "listing_expiration_date": "20261231"}