Package 72789-143-30

Brand: pravastatin sodium

Generic: pravastatin sodium
NDC Package

Package Facts

Identity

Package NDC 72789-143-30
Digits Only 7278914330
Product NDC 72789-143
Product ID 72789-143_2d686029-d11c-3f24-e063-6394a90aae0c
Description

30 TABLET in 1 BOTTLE, PLASTIC (72789-143-30)

Marketing

Marketing Status
Marketed Since 2020-10-22
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": "2d686029-d11c-3f24-e063-6394a90aae0c", "openfda": {"upc": ["0372789143309"], "unii": ["3M8608UQ61"], "rxcui": ["904467"], "spl_set_id": ["c5f611aa-9974-422e-a353-5d834a33937c"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (72789-143-30)", "package_ndc": "72789-143-30", "marketing_start_date": "20201022"}], "brand_name": "PRAVASTATIN SODIUM", "product_id": "72789-143_2d686029-d11c-3f24-e063-6394a90aae0c", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "72789-143", "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": "ANDA076341", "marketing_category": "ANDA", "marketing_start_date": "20110718", "listing_expiration_date": "20261231"}