Package 70518-0948-1

Brand: prednisone

Generic: prednisone
NDC Package

Package Facts

Identity

Package NDC 70518-0948-1
Digits Only 7051809481
Product NDC 70518-0948
Description

20 TABLET in 1 BOTTLE, PLASTIC (70518-0948-1)

Marketing

Marketing Status
Discontinued 2026-05-01
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": "4848f7d4-f1f9-b929-e063-6394a90a710d", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["VB0R961HZT"], "rxcui": ["312615"], "spl_set_id": ["612da092-033f-46a0-b49e-3f7809fafd2a"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE, PLASTIC (70518-0948-1)", "package_ndc": "70518-0948-1", "marketing_end_date": "20260501", "marketing_start_date": "20230815"}], "brand_name": "Prednisone", "product_id": "70518-0948_4848f7d4-f1f9-b929-e063-6394a90a710d", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "70518-0948", "generic_name": "Prednisone", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prednisone", "active_ingredients": [{"name": "PREDNISONE", "strength": "20 mg/1"}], "application_number": "ANDA040362", "marketing_category": "ANDA", "marketing_end_date": "20260501", "marketing_start_date": "20180110"}