Package 68071-3581-1

Brand: prednisone

Generic: prednisone
NDC Package

Package Facts

Identity

Package NDC 68071-3581-1
Digits Only 6807135811
Product NDC 68071-3581
Description

100 TABLET in 1 BOTTLE (68071-3581-1)

Marketing

Marketing Status
Marketed Since 2024-02-29
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": "1289ccc0-8def-ceab-e063-6294a90ac106", "openfda": {"nui": ["N0000175576", "N0000175450"], "upc": ["0368071358117"], "unii": ["VB0R961HZT"], "rxcui": ["312617"], "spl_set_id": ["1289c6d2-2707-baca-e063-6294a90a750d"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68071-3581-1)", "package_ndc": "68071-3581-1", "marketing_start_date": "20240229"}], "brand_name": "PredniSONE", "product_id": "68071-3581_1289ccc0-8def-ceab-e063-6294a90ac106", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "68071-3581", "generic_name": "PredniSONE", "labeler_name": "NuCare Pharmaceuticals,Inc.", "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"}