Package 0904-6923-61

Brand: prednisone

Generic: prednisone
NDC Package

Package Facts

Identity

Package NDC 0904-6923-61
Digits Only 0904692361
Product NDC 0904-6923
Description

100 BLISTER PACK in 1 CARTON (0904-6923-61) / 1 TABLET in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2002-07-12
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": "4eedc509-491a-40f4-b428-020497062d17", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["VB0R961HZT"], "rxcui": ["198145"], "spl_set_id": ["57b98930-92ab-4b77-a033-ae9895ee718a"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-6923-61)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "0904-6923-61", "marketing_start_date": "20020712"}], "brand_name": "Prednisone", "product_id": "0904-6923_4eedc509-491a-40f4-b428-020497062d17", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "0904-6923", "generic_name": "Prednisone", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prednisone", "active_ingredients": [{"name": "PREDNISONE", "strength": "10 mg/1"}], "application_number": "ANDA040256", "marketing_category": "ANDA", "marketing_start_date": "20020712", "listing_expiration_date": "20261231"}