Package 80425-0069-1

Brand: prednisone

Generic: prednisone
NDC Package

Package Facts

Identity

Package NDC 80425-0069-1
Digits Only 8042500691
Product NDC 80425-0069
Product ID 80425-0069_2a98d9c1-b774-40b1-e063-6294a90a20e4
Description

21 TABLET in 1 BOTTLE (80425-0069-1)

Marketing

Marketing Status
Marketed Since 2001-08-29
Brand prednisone
Generic prednisone
Sample Package No

Linked Drug Pages (1)

Prednisone ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2a98d9c1-b774-40b1-e063-6294a90a20e4", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["VB0R961HZT"], "rxcui": ["312617"], "spl_set_id": ["af863b9e-964b-3b1e-e053-2995a90ab93a"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["Advanced Rx of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "21 TABLET in 1 BOTTLE (80425-0069-1)", "package_ndc": "80425-0069-1", "marketing_start_date": "20010829"}], "brand_name": "Prednisone", "product_id": "80425-0069_2a98d9c1-b774-40b1-e063-6294a90a20e4", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "80425-0069", "generic_name": "Prednisone", "labeler_name": "Advanced Rx of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prednisone", "active_ingredients": [{"name": "PREDNISONE", "strength": "5 mg/1"}], "application_number": "ANDA040362", "marketing_category": "ANDA", "marketing_start_date": "20010829", "listing_expiration_date": "20261231"}