Package 67046-1610-3

Brand: prednisone

Generic: prednisone
NDC Package

Package Facts

Identity

Package NDC 67046-1610-3
Digits Only 6704616103
Product NDC 67046-1610
Description

30 TABLET in 1 BLISTER PACK (67046-1610-3)

Marketing

Marketing Status
Marketed Since 2025-10-24
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": "41e71126-b6bf-cef1-e063-6394a90a800d", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["VB0R961HZT"], "rxcui": ["312615"], "spl_set_id": ["41e6f1c3-d225-0ff0-e063-6394a90ace88"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (67046-1610-3)", "package_ndc": "67046-1610-3", "marketing_start_date": "20251024"}], "brand_name": "PREDNISONE", "product_id": "67046-1610_41e71126-b6bf-cef1-e063-6394a90a800d", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "67046-1610", "generic_name": "PREDNISONE", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PREDNISONE", "active_ingredients": [{"name": "PREDNISONE", "strength": "20 mg/1"}], "application_number": "ANDA215672", "marketing_category": "ANDA", "marketing_start_date": "20251024", "listing_expiration_date": "20261231"}