Package 72789-161-30

Brand: pravastatin sodium

Generic: pravastatin sodium
NDC Package

Package Facts

Identity

Package NDC 72789-161-30
Digits Only 7278916130
Product NDC 72789-161
Product ID 72789-161_4af789d1-0ff2-b237-e063-6294a90a6e52
Description

30 TABLET in 1 BOTTLE, PLASTIC (72789-161-30)

Marketing

Marketing Status
Marketed Since 2021-01-26
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": "4af789d1-0ff2-b237-e063-6294a90a6e52", "openfda": {"upc": ["0372789161303"], "unii": ["3M8608UQ61"], "rxcui": ["904475"], "spl_set_id": ["8dbdc80d-9d8c-4e22-9108-d87a77e07a6b"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (72789-161-30)", "package_ndc": "72789-161-30", "marketing_start_date": "20210126"}], "brand_name": "PRAVASTATIN SODIUM", "product_id": "72789-161_4af789d1-0ff2-b237-e063-6294a90a6e52", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "72789-161", "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": "40 mg/1"}], "application_number": "ANDA076341", "marketing_category": "ANDA", "marketing_start_date": "20110718", "listing_expiration_date": "20271231"}