Package 70518-4354-0

Brand: prednisone

Generic: prednisone
NDC Package

Package Facts

Identity

Package NDC 70518-4354-0
Digits Only 7051843540
Product NDC 70518-4354
Description

30 TABLET in 1 BLISTER PACK (70518-4354-0)

Marketing

Marketing Status
Marketed Since 2025-06-09
Brand prednisone
Generic prednisone
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3738d71b-07cf-dfa2-e063-6294a90a7f74", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["VB0R961HZT"], "rxcui": ["198145"], "spl_set_id": ["4750028a-30ad-420a-8e6b-06dc2429d433"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-4354-0)", "package_ndc": "70518-4354-0", "marketing_start_date": "20250609"}], "brand_name": "prednisone", "product_id": "70518-4354_3738d71b-07cf-dfa2-e063-6294a90a7f74", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "70518-4354", "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": "ANDA213386", "marketing_category": "ANDA", "marketing_start_date": "20250609", "listing_expiration_date": "20261231"}