Package 82009-007-10
Brand: pravastatin sodium
Generic: pravastatin sodiumPackage Facts
Identity
Package NDC
82009-007-10
Digits Only
8200900710
Product NDC
82009-007
Description
1000 TABLET in 1 BOTTLE (82009-007-10)
Marketing
Marketing Status
Brand
pravastatin sodium
Generic
pravastatin sodium
Sample Package
No
Linked Drug Pages (0)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "edcdc136-1cb4-26ac-2dc7-fcf26c4b5319", "openfda": {"unii": ["3M8608UQ61"], "rxcui": ["904467", "904475", "904481"], "spl_set_id": ["e9c188f7-cd6f-afac-b493-36552d86589e"], "manufacturer_name": ["Quallent"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (82009-007-10)", "package_ndc": "82009-007-10", "marketing_start_date": "20211203"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (82009-007-90)", "package_ndc": "82009-007-90", "marketing_start_date": "20211203"}], "brand_name": "PRAVASTATIN SODIUM", "product_id": "82009-007_edcdc136-1cb4-26ac-2dc7-fcf26c4b5319", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "82009-007", "generic_name": "PRAVASTATIN SODIUM", "labeler_name": "Quallent", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PRAVASTATIN SODIUM", "active_ingredients": [{"name": "PRAVASTATIN SODIUM", "strength": "40 mg/1"}], "application_number": "ANDA076341", "marketing_category": "ANDA", "marketing_start_date": "20211203", "listing_expiration_date": "20261231"}