Package 68071-3821-3

Brand: prednisone

Generic: prednisone
NDC Package

Package Facts

Identity

Package NDC 68071-3821-3
Digits Only 6807138213
Product NDC 68071-3821
Description

30 TABLET in 1 BOTTLE (68071-3821-3)

Marketing

Marketing Status
Marketed Since 2025-04-02
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": "31cfbc07-b041-ad9d-e063-6394a90ab204", "openfda": {"nui": ["N0000175576", "N0000175450"], "upc": ["0368071382136"], "unii": ["VB0R961HZT"], "rxcui": ["198145"], "spl_set_id": ["31cfc21f-726b-ae80-e063-6294a90a9af4"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68071-3821-3)", "package_ndc": "68071-3821-3", "marketing_start_date": "20250402"}], "brand_name": "Prednisone", "product_id": "68071-3821_31cfbc07-b041-ad9d-e063-6394a90ab204", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "68071-3821", "generic_name": "Prednisone", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prednisone", "active_ingredients": [{"name": "PREDNISONE", "strength": "10 mg/1"}], "application_number": "ANDA211575", "marketing_category": "ANDA", "marketing_start_date": "20191115", "listing_expiration_date": "20261231"}