Package 42708-166-21

Brand: prednisone

Generic: prednisone
NDC Package Sample

Package Facts

Identity

Package NDC 42708-166-21
Digits Only 4270816621
Product NDC 42708-166
Product ID 42708-166_459bc967-8124-16f1-e063-6394a90aa539
Description

21 TABLET in 1 BOTTLE, PLASTIC (42708-166-21)

Marketing

Marketing Status
Marketed Since 2023-03-24
Brand prednisone
Generic prednisone
Sample Package Yes

Linked Drug Pages (1)

prednisone ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "459bc967-8124-16f1-e063-6394a90aa539", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["VB0R961HZT"], "rxcui": ["198145"], "spl_set_id": ["f795ea1d-f41a-6100-e053-6394a90a63a4"], "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 (42708-166-21)", "package_ndc": "42708-166-21", "marketing_start_date": "20230324"}], "brand_name": "prednisone", "product_id": "42708-166_459bc967-8124-16f1-e063-6394a90aa539", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "42708-166", "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": "ANDA208412", "marketing_category": "ANDA", "marketing_start_date": "20210901", "listing_expiration_date": "20261231"}