Package 70518-4560-0

Brand: prednisone

Generic: prednisone
NDC Package

Package Facts

Identity

Package NDC 70518-4560-0
Digits Only 7051845600
Product NDC 70518-4560
Description

18 TABLET in 1 BOTTLE, PLASTIC (70518-4560-0)

Marketing

Marketing Status
Marketed Since 2026-02-02
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": "49dd8f0d-8dde-d9d2-e063-6394a90aa173", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["VB0R961HZT"], "rxcui": ["198145"], "spl_set_id": ["ab9bffed-b1a2-4e82-ac45-bee40b41060f"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "18 TABLET in 1 BOTTLE, PLASTIC (70518-4560-0)", "package_ndc": "70518-4560-0", "marketing_start_date": "20260202"}], "brand_name": "PREDNISONE", "product_id": "70518-4560_49dd8f0d-8dde-d9d2-e063-6394a90aa173", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "70518-4560", "generic_name": "PREDNISONE", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PREDNISONE", "active_ingredients": [{"name": "PREDNISONE", "strength": "10 mg/1"}], "application_number": "ANDA215672", "marketing_category": "ANDA", "marketing_start_date": "20260202", "listing_expiration_date": "20271231"}