Package 50090-2024-0

Brand: pravastatin sodium

Generic: pravastatin sodium
NDC Package

Package Facts

Identity

Package NDC 50090-2024-0
Digits Only 5009020240
Product NDC 50090-2024
Description

30 TABLET in 1 BOTTLE (50090-2024-0)

Marketing

Marketing Status
Marketed Since 2015-09-23
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": "2b4060ff-7a7c-4bf4-956e-c0e45a3d3252", "openfda": {"unii": ["3M8608UQ61"], "rxcui": ["904467", "904475"], "spl_set_id": ["93b0e546-9e0f-40d1-9b1e-082bf16400a4"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-2024-0)", "package_ndc": "50090-2024-0", "marketing_start_date": "20150923"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-2024-1)", "package_ndc": "50090-2024-1", "marketing_start_date": "20150923"}], "brand_name": "PRAVASTATIN SODIUM", "product_id": "50090-2024_2b4060ff-7a7c-4bf4-956e-c0e45a3d3252", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "50090-2024", "generic_name": "PRAVASTATIN SODIUM", "labeler_name": "A-S Medication Solutions", "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": "20110718", "listing_expiration_date": "20261231"}