Package 0603-5335-32

Brand: prednisone

Generic: prednisone
NDC Package

Package Facts

Identity

Package NDC 0603-5335-32
Digits Only 0603533532
Product NDC 0603-5335
Description

1000 TABLET in 1 BOTTLE, PLASTIC (0603-5335-32)

Marketing

Marketing Status
Marketed Since 2004-12-21
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": "e6628b5c-a3e4-462b-a01a-695ed8d3ab64", "openfda": {"nui": ["N0000175576", "N0000175450"], "upc": ["0306035335217", "0306035339215", "0306035338218"], "unii": ["VB0R961HZT"], "rxcui": ["198144", "198145", "198146", "312615", "312617", "763179", "763181", "763183", "763185"], "spl_set_id": ["10fe5a3b-84dc-4600-87c2-b80c97ce18cf"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["Endo USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (0603-5335-21)", "package_ndc": "0603-5335-21", "marketing_start_date": "20041221"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE, PLASTIC (0603-5335-32)", "package_ndc": "0603-5335-32", "marketing_start_date": "20041221"}], "brand_name": "Prednisone", "product_id": "0603-5335_e6628b5c-a3e4-462b-a01a-695ed8d3ab64", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "0603-5335", "generic_name": "Prednisone", "labeler_name": "Endo USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prednisone", "active_ingredients": [{"name": "PREDNISONE", "strength": "1 mg/1"}], "application_number": "ANDA040584", "marketing_category": "ANDA", "marketing_start_date": "20041221", "listing_expiration_date": "20261231"}