Package 43353-964-45

Brand: pravastatin sodium

Generic: pravastatin sodium
NDC Package

Package Facts

Identity

Package NDC 43353-964-45
Digits Only 4335396445
Product NDC 43353-964
Product ID 43353-964_0d6fa0b8-bef8-42ff-8b4e-ea21b291a8e2
Description

45 TABLET in 1 BOTTLE (43353-964-45)

Marketing

Marketing Status
Marketed Since 2014-09-26
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": "0d6fa0b8-bef8-42ff-8b4e-ea21b291a8e2", "openfda": {"unii": ["3M8608UQ61"], "rxcui": ["904475", "904481"], "spl_set_id": ["576f2e65-2bf6-4f6b-8538-50221f2d88bb"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "45 TABLET in 1 BOTTLE (43353-964-45)", "package_ndc": "43353-964-45", "marketing_start_date": "20140926"}], "brand_name": "Pravastatin Sodium", "product_id": "43353-964_0d6fa0b8-bef8-42ff-8b4e-ea21b291a8e2", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "43353-964", "generic_name": "Pravastatin Sodium", "labeler_name": "Aphena Pharma Solutions - Tennessee, 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": "20140617", "listing_expiration_date": "20261231"}