Package 42658-160-05

Brand: prednisolone

Generic: prednisolone
NDC Package

Package Facts

Identity

Package NDC 42658-160-05
Digits Only 4265816005
Product NDC 42658-160
Description

100 TABLET in 1 BOTTLE (42658-160-05)

Marketing

Marketing Status
Marketed Since 2024-09-01
Brand prednisolone
Generic prednisolone
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "9f93400d-a8c0-435a-ad65-48717cc455cf", "openfda": {"nui": ["N0000175576", "N0000175450"], "upc": ["0342658160058"], "unii": ["9PHQ9Y1OLM"], "rxcui": ["198142"], "spl_set_id": ["16d4e064-66d3-4497-8c7d-3aa355f91e1d"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["Hisun Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (42658-160-05)", "package_ndc": "42658-160-05", "marketing_start_date": "20240901"}], "brand_name": "PREDNISOLONE", "product_id": "42658-160_9f93400d-a8c0-435a-ad65-48717cc455cf", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "42658-160", "generic_name": "PREDNISOLONE", "labeler_name": "Hisun Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PREDNISOLONE", "active_ingredients": [{"name": "PREDNISOLONE", "strength": "5 mg/1"}], "application_number": "ANDA218083", "marketing_category": "ANDA", "marketing_start_date": "20240901", "listing_expiration_date": "20261231"}