Package 63629-8833-1

Brand: pravastatin sodium

Generic: pravastatin sodium
NDC Package

Package Facts

Identity

Package NDC 63629-8833-1
Digits Only 6362988331
Product NDC 63629-8833
Description

90 TABLET in 1 BOTTLE (63629-8833-1)

Marketing

Marketing Status
Marketed Since 2011-07-18
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": "167a2550-ca7b-4990-8c0f-5922af045614", "openfda": {"unii": ["3M8608UQ61"], "rxcui": ["904458"], "spl_set_id": ["2ba7af14-9c87-4eb0-84c9-7e895cd75fae"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (63629-8833-1)", "package_ndc": "63629-8833-1", "marketing_start_date": "20110718"}], "brand_name": "PRAVASTATIN SODIUM", "product_id": "63629-8833_167a2550-ca7b-4990-8c0f-5922af045614", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "63629-8833", "generic_name": "PRAVASTATIN SODIUM", "labeler_name": "Bryant Ranch Prepack", "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": "20110718", "listing_expiration_date": "20261231"}