Package 72789-448-21

Brand: prednisone

Generic: prednisone
NDC Package

Package Facts

Identity

Package NDC 72789-448-21
Digits Only 7278944821
Product NDC 72789-448
Description

21 TABLET in 1 BOTTLE, PLASTIC (72789-448-21)

Marketing

Marketing Status
Marketed Since 2024-10-30
Brand prednisone
Generic prednisone
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2e8259e9-0872-8e19-e063-6294a90ab084", "openfda": {"nui": ["N0000175576", "N0000175450"], "upc": ["0372789448213"], "unii": ["VB0R961HZT"], "rxcui": ["312615"], "spl_set_id": ["25b5958b-c151-9200-e063-6394a90af52c"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "21 TABLET in 1 BOTTLE, PLASTIC (72789-448-21)", "package_ndc": "72789-448-21", "marketing_start_date": "20241030"}], "brand_name": "Prednisone", "product_id": "72789-448_2e8259e9-0872-8e19-e063-6294a90ab084", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "72789-448", "generic_name": "Prednisone", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prednisone", "active_ingredients": [{"name": "PREDNISONE", "strength": "20 mg/1"}], "application_number": "ANDA211575", "marketing_category": "ANDA", "marketing_start_date": "20191115", "listing_expiration_date": "20261231"}