Package 72789-500-21
Brand: prednisone tablets, usp, 20 mg
Generic: prednisonePackage Facts
Identity
Package NDC
72789-500-21
Digits Only
7278950021
Product NDC
72789-500
Description
21 TABLET in 1 BOTTLE, PLASTIC (72789-500-21)
Marketing
Marketing Status
Brand
prednisone tablets, usp, 20 mg
Generic
prednisone
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "38438a7a-984c-7109-e063-6394a90a0a32", "openfda": {"nui": ["N0000175576", "N0000175450"], "upc": ["0372789500218"], "unii": ["VB0R961HZT"], "rxcui": ["312615"], "spl_set_id": ["3befbdc5-7d20-41b6-ad80-98e1c6b8caf5"], "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 (72789-500-21)", "package_ndc": "72789-500-21", "marketing_start_date": "20250522"}], "brand_name": "PredniSONE Tablets, USP, 20 mg", "product_id": "72789-500_38438a7a-984c-7109-e063-6394a90a0a32", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "72789-500", "generic_name": "PredniSONE", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PredniSONE Tablets, USP, 20 mg", "active_ingredients": [{"name": "PREDNISONE", "strength": "20 mg/1"}], "application_number": "ANDA212629", "marketing_category": "ANDA", "marketing_start_date": "20250522", "listing_expiration_date": "20261231"}