Package 70518-0549-0

Brand: pravastatin sodium

Generic: pravastatin sodium
NDC Package

Package Facts

Identity

Package NDC 70518-0549-0
Digits Only 7051805490
Product NDC 70518-0549
Product ID 70518-0549_47f8b1ff-cf4e-86b9-e063-6394a90a7dc0
Description

30 TABLET in 1 BLISTER PACK (70518-0549-0)

Marketing

Marketing Status
Marketed Since 2017-05-19
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": "47f8b1ff-cf4e-86b9-e063-6394a90a7dc0", "openfda": {"unii": ["3M8608UQ61"], "rxcui": ["904458"], "spl_set_id": ["76e5fdf8-bd03-4cd5-9361-e61678cb3de9"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-0549-0)", "package_ndc": "70518-0549-0", "marketing_start_date": "20170519"}], "brand_name": "PRAVASTATIN SODIUM", "product_id": "70518-0549_47f8b1ff-cf4e-86b9-e063-6394a90a7dc0", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "70518-0549", "generic_name": "PRAVASTATIN SODIUM", "labeler_name": "REMEDYREPACK 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": "20170519", "listing_expiration_date": "20271231"}