Package 43063-807-30

Brand: pravastatin sodium

Generic: pravastatin sodium
NDC Package

Package Facts

Identity

Package NDC 43063-807-30
Digits Only 4306380730
Product NDC 43063-807
Product ID 43063-807_415b92e7-5f31-108d-e063-6394a90a5452
Description

30 TABLET in 1 BOTTLE, PLASTIC (43063-807-30)

Marketing

Marketing Status
Marketed Since 2017-02-16
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": "415b92e7-5f31-108d-e063-6394a90a5452", "openfda": {"unii": ["3M8608UQ61"], "rxcui": ["904467"], "spl_set_id": ["2ded7e5e-c377-4495-a045-f1c57b90c5db"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (43063-807-30)", "package_ndc": "43063-807-30", "marketing_start_date": "20170216"}], "brand_name": "PRAVASTATIN SODIUM", "product_id": "43063-807_415b92e7-5f31-108d-e063-6394a90a5452", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "43063-807", "generic_name": "PRAVASTATIN SODIUM", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PRAVASTATIN SODIUM", "active_ingredients": [{"name": "PRAVASTATIN SODIUM", "strength": "20 mg/1"}], "application_number": "ANDA207068", "marketing_category": "ANDA", "marketing_start_date": "20170216", "listing_expiration_date": "20261231"}