Package 72189-593-21

Brand: prednisone

Generic: prednisone
NDC Package

Package Facts

Identity

Package NDC 72189-593-21
Digits Only 7218959321
Product NDC 72189-593
Product ID 72189-593_26194836-90ca-6909-e063-6294a90a6f98
Description

21 TABLET in 1 BOTTLE (72189-593-21)

Marketing

Marketing Status
Marketed Since 2024-11-04
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": "26194836-90ca-6909-e063-6294a90a6f98", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["VB0R961HZT"], "rxcui": ["312617"], "spl_set_id": ["26194836-90c9-6909-e063-6294a90a6f98"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "21 TABLET in 1 BOTTLE (72189-593-21)", "package_ndc": "72189-593-21", "marketing_start_date": "20241104"}], "brand_name": "Prednisone", "product_id": "72189-593_26194836-90ca-6909-e063-6294a90a6f98", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "72189-593", "generic_name": "Prednisone", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prednisone", "active_ingredients": [{"name": "PREDNISONE", "strength": "5 mg/1"}], "application_number": "ANDA209727", "marketing_category": "ANDA", "marketing_start_date": "20241104", "listing_expiration_date": "20261231"}