prednisone
Generic: prednisone
Labeler: northwind health company, llcDrug Facts
Product Profile
Brand Name
prednisone
Generic Name
prednisone
Labeler
northwind health company, llc
Dosage Form
TABLET
Routes
Active Ingredients
prednisone 50 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
51655-359
Product ID
51655-359_48eb80e1-ee3a-10b3-e063-6294a90a5180
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA211575
Listing Expiration
2027-12-31
Marketing Start
2023-05-09
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
51655359
Hyphenated Format
51655-359
Supplemental Identifiers
RxCUI
UNII
NUI
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
prednisone (source: ndc)
Generic Name
prednisone (source: ndc)
Application Number
ANDA211575 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 mg/1
Packaging
- 5 TABLET in 1 BOTTLE, PLASTIC (51655-359-55)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "48eb80e1-ee3a-10b3-e063-6294a90a5180", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["VB0R961HZT"], "rxcui": ["198148"], "spl_set_id": ["fbd3f0c3-06b3-c9b4-e053-6294a90a6fdd"], "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": "5 TABLET in 1 BOTTLE, PLASTIC (51655-359-55)", "package_ndc": "51655-359-55", "marketing_start_date": "20230509"}], "brand_name": "Prednisone", "product_id": "51655-359_48eb80e1-ee3a-10b3-e063-6294a90a5180", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "51655-359", "generic_name": "Prednisone", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prednisone", "active_ingredients": [{"name": "PREDNISONE", "strength": "50 mg/1"}], "application_number": "ANDA211575", "marketing_category": "ANDA", "marketing_start_date": "20230509", "listing_expiration_date": "20271231"}