Package 72189-646-21

Brand: prednisone d/p

Generic: prednisone d/p
NDC Package

Package Facts

Identity

Package NDC 72189-646-21
Digits Only 7218964621
Product NDC 72189-646
Description

21 TABLET in 1 CARTON (72189-646-21)

Marketing

Marketing Status
Marketed Since 2025-10-21
Brand prednisone d/p
Generic prednisone d/p
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "41ade439-59f3-dfd1-e063-6294a90aca0f", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["VB0R961HZT"], "rxcui": ["198145", "763185"], "spl_set_id": ["41ade439-59f2-dfd1-e063-6294a90aca0f"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "21 TABLET in 1 CARTON (72189-646-21)", "package_ndc": "72189-646-21", "marketing_start_date": "20251021"}], "brand_name": "Prednisone D/P", "product_id": "72189-646_41ade439-59f3-dfd1-e063-6294a90aca0f", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "72189-646", "generic_name": "Prednisone D/P", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prednisone D/P", "active_ingredients": [{"name": "PREDNISONE", "strength": "10 mg/1"}], "application_number": "ANDA085162", "marketing_category": "ANDA", "marketing_start_date": "20251021", "listing_expiration_date": "20261231"}