Package 60760-796-21

Brand: prednisone

Generic: prednisone
NDC Package

Package Facts

Identity

Package NDC 60760-796-21
Digits Only 6076079621
Product NDC 60760-796
Description

21 TABLET in 1 BOTTLE, PLASTIC (60760-796-21)

Marketing

Marketing Status
Marketed Since 2024-04-09
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": "16ee68eb-d166-3dc2-e063-6394a90aabd7", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["VB0R961HZT"], "rxcui": ["312617"], "spl_set_id": ["16ee689e-c7a9-3a5a-e063-6394a90a6ea2"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["ST. MARY'S MEDICAL PARK PHARMACY"]}, "finished": true, "packaging": [{"sample": false, "description": "21 TABLET in 1 BOTTLE, PLASTIC (60760-796-21)", "package_ndc": "60760-796-21", "marketing_start_date": "20240409"}], "brand_name": "PredniSONE", "product_id": "60760-796_16ee68eb-d166-3dc2-e063-6394a90aabd7", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "60760-796", "generic_name": "PredniSONE", "labeler_name": "ST. MARY'S MEDICAL PARK PHARMACY", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PredniSONE", "active_ingredients": [{"name": "PREDNISONE", "strength": "5 mg/1"}], "application_number": "ANDA080352", "marketing_category": "ANDA", "marketing_start_date": "20200323", "listing_expiration_date": "20261231"}