Package 72189-059-90

Brand: pravastatin sodium

Generic: pravastatin sodium
NDC Package

Package Facts

Identity

Package NDC 72189-059-90
Digits Only 7218905990
Product NDC 72189-059
Product ID 72189-059_2be8f6ba-328a-86ab-e063-6394a90acb89
Description

90 TABLET in 1 BOTTLE (72189-059-90)

Marketing

Marketing Status
Marketed Since 2019-11-11
Brand pravastatin sodium
Generic pravastatin sodium
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2be8f6ba-328a-86ab-e063-6394a90acb89", "openfda": {"unii": ["3M8608UQ61"], "rxcui": ["904458", "904467", "904475", "904481"], "spl_set_id": ["97178675-3691-2d93-e053-2995a90aa5c1"], "manufacturer_name": ["DIRECT RX"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (72189-059-90)", "package_ndc": "72189-059-90", "marketing_start_date": "20191111"}], "brand_name": "PRAVASTATIN SODIUM", "product_id": "72189-059_2be8f6ba-328a-86ab-e063-6394a90acb89", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "72189-059", "generic_name": "PRAVASTATIN SODIUM", "labeler_name": "DIRECT RX", "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": "20191111", "listing_expiration_date": "20261231"}