Package 50090-3204-0

Brand: pravastatin sodium

Generic: pravastatin sodium
NDC Package

Package Facts

Identity

Package NDC 50090-3204-0
Digits Only 5009032040
Product NDC 50090-3204
Description

30 TABLET in 1 BOTTLE (50090-3204-0)

Marketing

Marketing Status
Marketed Since 2017-10-23
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": "4ff259d6-5a83-482d-9e02-08fa0bf3ce08", "openfda": {"unii": ["3M8608UQ61"], "rxcui": ["904481"], "spl_set_id": ["7b4ef7a8-47e5-428f-91de-7307dcbb9167"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-3204-0)", "package_ndc": "50090-3204-0", "marketing_start_date": "20171023"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (50090-3204-1)", "package_ndc": "50090-3204-1", "marketing_start_date": "20141128"}], "brand_name": "PRAVASTATIN SODIUM", "product_id": "50090-3204_4ff259d6-5a83-482d-9e02-08fa0bf3ce08", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "50090-3204", "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": "80 mg/1"}], "application_number": "ANDA076341", "marketing_category": "ANDA", "marketing_start_date": "20110718", "listing_expiration_date": "20261231"}