Package 68071-3361-9

Brand: pravastatin sodium

Generic: pravastatin sodium
NDC Package

Package Facts

Identity

Package NDC 68071-3361-9
Digits Only 6807133619
Product NDC 68071-3361
Description

90 TABLET in 1 BOTTLE (68071-3361-9)

Marketing

Marketing Status
Marketed Since 2017-07-12
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": "1ce9135a-5f51-1bdf-e063-6294a90a0164", "openfda": {"upc": ["0368071336191"], "unii": ["3M8608UQ61"], "rxcui": ["904467"], "spl_set_id": ["54228087-7ab0-5561-e054-00144ff8d46c"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68071-3361-3)", "package_ndc": "68071-3361-3", "marketing_start_date": "20170712"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68071-3361-9)", "package_ndc": "68071-3361-9", "marketing_start_date": "20170712"}], "brand_name": "PRAVASTATIN SODIUM", "product_id": "68071-3361_1ce9135a-5f51-1bdf-e063-6294a90a0164", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "68071-3361", "generic_name": "PRAVASTATIN SODIUM", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PRAVASTATIN SODIUM", "active_ingredients": [{"name": "PRAVASTATIN SODIUM", "strength": "20 mg/1"}], "application_number": "ANDA076341", "marketing_category": "ANDA", "marketing_start_date": "20110718", "listing_expiration_date": "20261231"}