Package 42708-045-21

Brand: prednisone

Generic: prednisone
NDC Package Sample

Package Facts

Identity

Package NDC 42708-045-21
Digits Only 4270804521
Product NDC 42708-045
Description

21 TABLET in 1 BOTTLE, PLASTIC (42708-045-21)

Marketing

Marketing Status
Marketed Since 2018-03-17
Brand prednisone
Generic prednisone
Sample Package Yes

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "45b3e0e2-7ec6-7419-e063-6394a90a2f2a", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["VB0R961HZT"], "rxcui": ["198145"], "spl_set_id": ["318fdf0d-c03a-4b48-a380-b7bb630363fb"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["QPharma, Inc."]}, "finished": true, "packaging": [{"sample": true, "description": "21 TABLET in 1 BOTTLE, PLASTIC (42708-045-21)", "package_ndc": "42708-045-21", "marketing_start_date": "20180317"}], "brand_name": "PredniSONE", "product_id": "42708-045_45b3e0e2-7ec6-7419-e063-6394a90a2f2a", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "42708-045", "generic_name": "PredniSONE", "labeler_name": "QPharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PredniSONE", "active_ingredients": [{"name": "PREDNISONE", "strength": "10 mg/1"}], "application_number": "ANDA084122", "marketing_category": "ANDA", "marketing_start_date": "20030213", "listing_expiration_date": "20261231"}