Package 50090-3853-0

Brand: pravastatin sodium

Generic: pravastatin sodium
NDC Package

Package Facts

Identity

Package NDC 50090-3853-0
Digits Only 5009038530
Product NDC 50090-3853
Description

90 TABLET in 1 BOTTLE (50090-3853-0)

Marketing

Marketing Status
Marketed Since 2018-11-21
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": "10559b70-d5be-41e8-a456-cbaa4753b604", "openfda": {"unii": ["3M8608UQ61"], "rxcui": ["904458"], "spl_set_id": ["3e6d1c1e-d5f7-42ec-bcdd-8fc310acdf21"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-3853-0)", "package_ndc": "50090-3853-0", "marketing_start_date": "20181121"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-3853-1)", "package_ndc": "50090-3853-1", "marketing_start_date": "20181121"}], "brand_name": "PRAVASTATIN SODIUM", "product_id": "50090-3853_10559b70-d5be-41e8-a456-cbaa4753b604", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "50090-3853", "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": "10 mg/1"}], "application_number": "ANDA076341", "marketing_category": "ANDA", "marketing_start_date": "20110718", "listing_expiration_date": "20271231"}