Package 72189-489-07

Brand: prednisone

Generic: prednisone
NDC Package

Package Facts

Identity

Package NDC 72189-489-07
Digits Only 7218948907
Product NDC 72189-489
Description

7 TABLET in 1 BOTTLE (72189-489-07)

Marketing

Marketing Status
Marketed Since 2023-06-07
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": "2c4e30d6-25ee-5c75-e063-6294a90a2fc2", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["VB0R961HZT"], "rxcui": ["198148"], "spl_set_id": ["fd8eb82e-52df-c368-e053-6294a90ac6b0"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "7 TABLET in 1 BOTTLE (72189-489-07)", "package_ndc": "72189-489-07", "marketing_start_date": "20230607"}], "brand_name": "Prednisone", "product_id": "72189-489_2c4e30d6-25ee-5c75-e063-6294a90a2fc2", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "72189-489", "generic_name": "Prednisone", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prednisone", "active_ingredients": [{"name": "PREDNISONE", "strength": "50 mg/1"}], "application_number": "ANDA208412", "marketing_category": "ANDA", "marketing_start_date": "20230607", "listing_expiration_date": "20261231"}