Package 71335-3046-1

Brand: prednisone tablets, usp, 20 mg

Generic: prednisone
NDC Package

Package Facts

Identity

Package NDC 71335-3046-1
Digits Only 7133530461
Product NDC 71335-3046
Description

100 TABLET in 1 BOTTLE (71335-3046-1)

Marketing

Marketing Status
Marketed Since 2025-12-03
Brand prednisone tablets, usp, 20 mg
Generic prednisone
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "d7d3a302-6908-482b-9d92-ef30ec37d10f", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["VB0R961HZT"], "rxcui": ["312615"], "spl_set_id": ["53bd04e8-6cbd-45f6-ac59-53fd3005a221"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-3046-1)", "package_ndc": "71335-3046-1", "marketing_start_date": "20251203"}], "brand_name": "PredniSONE Tablets, USP, 20 mg", "product_id": "71335-3046_d7d3a302-6908-482b-9d92-ef30ec37d10f", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "71335-3046", "generic_name": "PredniSONE", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PredniSONE Tablets, USP, 20 mg", "active_ingredients": [{"name": "PREDNISONE", "strength": "20 mg/1"}], "application_number": "ANDA212629", "marketing_category": "ANDA", "marketing_start_date": "20250522", "listing_expiration_date": "20261231"}