Package 84386-031-99

Brand: pravastatin sodium

Generic: pravastatin sodium
NDC Package

Package Facts

Identity

Package NDC 84386-031-99
Digits Only 8438603199
Product NDC 84386-031
Product ID 84386-031_cf6f7031-33b9-40d3-bc87-32f1b6af98f2
Description

1000 TABLET in 1 BOTTLE (84386-031-99)

Marketing

Marketing Status
Marketed Since 2025-02-27
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": "cf6f7031-33b9-40d3-bc87-32f1b6af98f2", "openfda": {"upc": ["0384386032900", "0384386031903", "0384386033907"], "unii": ["3M8608UQ61"], "rxcui": ["904458", "904467", "904475"], "spl_set_id": ["cf6f7031-33b9-40d3-bc87-32f1b6af98f2"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (84386-031-90)", "package_ndc": "84386-031-90", "marketing_start_date": "20250227"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (84386-031-99)", "package_ndc": "84386-031-99", "marketing_start_date": "20250227"}], "brand_name": "Pravastatin sodium", "product_id": "84386-031_cf6f7031-33b9-40d3-bc87-32f1b6af98f2", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "84386-031", "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": "10 mg/1"}], "application_number": "ANDA076056", "marketing_category": "ANDA", "marketing_start_date": "20250227", "listing_expiration_date": "20261231"}