Package 68071-5007-3

Brand: pravastatin sodium

Generic: pravastatin sodium
NDC Package

Package Facts

Identity

Package NDC 68071-5007-3
Digits Only 6807150073
Product NDC 68071-5007
Product ID 68071-5007_1b30df7b-a982-9706-e063-6394a90a5ea1
Description

30 TABLET in 1 BOTTLE (68071-5007-3)

Marketing

Marketing Status
Marketed Since 2019-07-29
Brand pravastatin sodium
Generic pravastatin sodium
Sample Package No

Linked Drug Pages (1)

PRAVASTATIN SODIUM ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1b30df7b-a982-9706-e063-6394a90a5ea1", "openfda": {"upc": ["0368071500738"], "unii": ["3M8608UQ61"], "rxcui": ["904458"], "spl_set_id": ["8ed7879d-988c-1a27-e053-2995a90a0361"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68071-5007-3)", "package_ndc": "68071-5007-3", "marketing_start_date": "20190729"}], "brand_name": "PRAVASTATIN SODIUM", "product_id": "68071-5007_1b30df7b-a982-9706-e063-6394a90a5ea1", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "68071-5007", "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": "10 mg/1"}], "application_number": "ANDA076341", "marketing_category": "ANDA", "marketing_start_date": "20110718", "listing_expiration_date": "20261231"}