Package 16729-008-16

Brand: pravastatin sodium

Generic: pravastatin sodium
NDC Package

Package Facts

Identity

Package NDC 16729-008-16
Digits Only 1672900816
Product NDC 16729-008
Description

500 TABLET in 1 BOTTLE (16729-008-16)

Marketing

Marketing Status
Marketed Since 2017-02-16
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": "438f9112-0851-75e1-e063-6294a90a675c", "openfda": {"unii": ["3M8608UQ61"], "rxcui": ["904458", "904467", "904475", "904481"], "spl_set_id": ["6c011348-a236-47d3-bbef-3e0b956dd080"], "manufacturer_name": ["Accord Healthcare Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (16729-008-15)", "package_ndc": "16729-008-15", "marketing_start_date": "20170216"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (16729-008-16)", "package_ndc": "16729-008-16", "marketing_start_date": "20170216"}], "brand_name": "PRAVASTATIN SODIUM", "product_id": "16729-008_438f9112-0851-75e1-e063-6294a90a675c", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "16729-008", "generic_name": "PRAVASTATIN SODIUM", "labeler_name": "Accord Healthcare Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PRAVASTATIN SODIUM", "active_ingredients": [{"name": "PRAVASTATIN SODIUM", "strength": "10 mg/1"}], "application_number": "ANDA207068", "marketing_category": "ANDA", "marketing_start_date": "20170216", "listing_expiration_date": "20261231"}