Package 51655-410-21
Brand: prednisone
Generic: prednisonePackage Facts
Identity
Package NDC
51655-410-21
Digits Only
5165541021
Product NDC
51655-410
Description
21 TABLET in 1 BOTTLE, PLASTIC (51655-410-21)
Marketing
Marketing Status
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": "48ff0341-60c9-05c3-e063-6294a90a031b", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["VB0R961HZT"], "rxcui": ["198145"], "spl_set_id": ["0f377d9f-b2f4-4dae-b503-5f963bea281f"], "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 (51655-410-20)", "package_ndc": "51655-410-20", "marketing_start_date": "20140428"}, {"sample": false, "description": "21 TABLET in 1 BOTTLE, PLASTIC (51655-410-21)", "package_ndc": "51655-410-21", "marketing_start_date": "20210610"}, {"sample": false, "description": "12 TABLET in 1 BOTTLE, PLASTIC (51655-410-27)", "package_ndc": "51655-410-27", "marketing_start_date": "20230303"}, {"sample": false, "description": "42 TABLET in 1 BOTTLE (51655-410-49)", "package_ndc": "51655-410-49", "marketing_start_date": "20140428"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (51655-410-52)", "package_ndc": "51655-410-52", "marketing_start_date": "20200410"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE, PLASTIC (51655-410-53)", "package_ndc": "51655-410-53", "marketing_start_date": "20230315"}, {"sample": false, "description": "15 TABLET in 1 BOTTLE, PLASTIC (51655-410-54)", "package_ndc": "51655-410-54", "marketing_start_date": "20210512"}], "brand_name": "Prednisone", "product_id": "51655-410_48ff0341-60c9-05c3-e063-6294a90a031b", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "51655-410", "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": "ANDA085162", "marketing_category": "ANDA", "marketing_start_date": "20140428", "listing_expiration_date": "20271231"}