Package 42708-115-21

Brand: prednisone

Generic: prednisone
NDC Package Sample

Package Facts

Identity

Package NDC 42708-115-21
Digits Only 4270811521
Product NDC 42708-115
Product ID 42708-115_459c17d6-14bb-9d87-e063-6294a90af969
Description

21 TABLET in 1 BOTTLE (42708-115-21)

Marketing

Marketing Status
Marketed Since 2018-04-20
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": "459c17d6-14bb-9d87-e063-6294a90af969", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["VB0R961HZT"], "rxcui": ["198145"], "spl_set_id": ["07fb8daa-2ceb-4564-b0d0-6cdf903da0b5"], "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 (42708-115-21)", "package_ndc": "42708-115-21", "marketing_start_date": "20180420"}], "brand_name": "Prednisone", "product_id": "42708-115_459c17d6-14bb-9d87-e063-6294a90af969", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "42708-115", "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": "ANDA085162", "marketing_category": "ANDA", "marketing_start_date": "19900101", "listing_expiration_date": "20261231"}