Package 51655-935-20

Brand: prednisone

Generic: prednisone
NDC Package

Package Facts

Identity

Package NDC 51655-935-20
Digits Only 5165593520
Product NDC 51655-935
Description

20 TABLET in 1 BOTTLE, PLASTIC (51655-935-20)

Marketing

Marketing Status
Marketed Since 2022-07-26
Brand prednisone
Generic prednisone
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "497447e4-31ff-bd8c-e063-6294a90a2398", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["VB0R961HZT"], "rxcui": ["198145"], "spl_set_id": ["f76db82a-826e-92b0-e053-6294a90a8ec6"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE, PLASTIC (51655-935-20)", "package_ndc": "51655-935-20", "marketing_start_date": "20220726"}], "brand_name": "Prednisone", "product_id": "51655-935_497447e4-31ff-bd8c-e063-6294a90a2398", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "51655-935", "generic_name": "Prednisone", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prednisone", "active_ingredients": [{"name": "PREDNISONE", "strength": "10 mg/1"}], "application_number": "ANDA088832", "marketing_category": "ANDA", "marketing_start_date": "20220726", "listing_expiration_date": "20271231"}