prednisone
Generic: prednisone
Labeler: medsource pharmaceuticalsDrug Facts
Product Profile
Brand Name
prednisone
Generic Name
prednisone
Labeler
medsource pharmaceuticals
Dosage Form
TABLET
Routes
Active Ingredients
prednisone 20 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
45865-884
Product ID
45865-884_13177b28-fa9d-9732-e063-6394a90ab442
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA208412
Listing Expiration
2026-12-31
Marketing Start
2021-09-01
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
45865884
Hyphenated Format
45865-884
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
ANDA208412 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/1
Packaging
- 21 TABLET in 1 BOTTLE (45865-884-21)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "13177b28-fa9d-9732-e063-6394a90ab442", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["VB0R961HZT"], "rxcui": ["312615"], "spl_set_id": ["131780a0-31f3-6588-e063-6294a90a2f8e"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["Medsource Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "21 TABLET in 1 BOTTLE (45865-884-21)", "package_ndc": "45865-884-21", "marketing_start_date": "20230324"}], "brand_name": "prednisone", "product_id": "45865-884_13177b28-fa9d-9732-e063-6394a90ab442", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "45865-884", "generic_name": "PREDNISONE", "labeler_name": "Medsource Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "prednisone", "active_ingredients": [{"name": "PREDNISONE", "strength": "20 mg/1"}], "application_number": "ANDA208412", "marketing_category": "ANDA", "marketing_start_date": "20210901", "listing_expiration_date": "20261231"}