Package 72162-1706-9

Brand: pravastatin sodium

Generic: pravastatin sodium
NDC Package

Package Facts

Identity

Package NDC 72162-1706-9
Digits Only 7216217069
Product NDC 72162-1706
Description

90 TABLET in 1 BOTTLE (72162-1706-9)

Marketing

Marketing Status
Marketed Since 2024-11-01
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": "94e20a25-4df5-4752-834f-a2881c673d49", "openfda": {"unii": ["3M8608UQ61"], "rxcui": ["904458"], "spl_set_id": ["f4b330ce-dfb0-4e4e-9f37-482458820c66"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72162-1706-3)", "package_ndc": "72162-1706-3", "marketing_start_date": "20241101"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (72162-1706-9)", "package_ndc": "72162-1706-9", "marketing_start_date": "20241101"}], "brand_name": "PRAVASTATIN SODIUM", "product_id": "72162-1706_94e20a25-4df5-4752-834f-a2881c673d49", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "72162-1706", "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"}