prednisone

Generic: prednisone

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name prednisone
Generic Name prednisone
Labeler a-s medication solutions
Dosage Form TABLET
Routes
ORAL
Active Ingredients

prednisone 10 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-7024
Product ID 50090-7024_a94e9e6b-45f2-4e67-aef0-bf0256e10406
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040256
Listing Expiration 2026-12-31
Marketing Start 2002-07-12

Pharmacologic Class

Established (EPC)
corticosteroid [epc]
Mechanism of Action
corticosteroid hormone receptor agonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500907024
Hyphenated Format 50090-7024

Supplemental Identifiers

RxCUI
198145
UNII
VB0R961HZT
NUI
N0000175576 N0000175450

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 ANDA040256 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 10 TABLET in 1 BOTTLE (50090-7024-0)
  • 15 TABLET in 1 BOTTLE (50090-7024-1)
  • 21 TABLET in 1 BOTTLE (50090-7024-2)
  • 50 TABLET in 1 BOTTLE (50090-7024-4)
  • 30 TABLET in 1 BOTTLE (50090-7024-5)
  • 40 TABLET in 1 BOTTLE (50090-7024-8)
source: ndc

Packages (6)

50090-7024-0 10 TABLET in 1 BOTTLE (50090-7024-0) 50090-7024-1 15 TABLET in 1 BOTTLE (50090-7024-1) 50090-7024-2 21 TABLET in 1 BOTTLE (50090-7024-2) 50090-7024-4 50 TABLET in 1 BOTTLE (50090-7024-4) 50090-7024-5 30 TABLET in 1 BOTTLE (50090-7024-5) 50090-7024-8 40 TABLET in 1 BOTTLE (50090-7024-8)

Ingredients (1)

prednisone (10 mg/1)

Linked Drug Pages (1)

Prednisone ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "a94e9e6b-45f2-4e67-aef0-bf0256e10406", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["VB0R961HZT"], "rxcui": ["198145"], "spl_set_id": ["44069d49-4cf4-4f1e-9fbd-b496c6ca81a1"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET in 1 BOTTLE (50090-7024-0)", "package_ndc": "50090-7024-0", "marketing_start_date": "20240108"}, {"sample": false, "description": "15 TABLET in 1 BOTTLE (50090-7024-1)", "package_ndc": "50090-7024-1", "marketing_start_date": "20240108"}, {"sample": false, "description": "21 TABLET in 1 BOTTLE (50090-7024-2)", "package_ndc": "50090-7024-2", "marketing_start_date": "20240108"}, {"sample": false, "description": "50 TABLET in 1 BOTTLE (50090-7024-4)", "package_ndc": "50090-7024-4", "marketing_start_date": "20240108"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-7024-5)", "package_ndc": "50090-7024-5", "marketing_start_date": "20240108"}, {"sample": false, "description": "40 TABLET in 1 BOTTLE (50090-7024-8)", "package_ndc": "50090-7024-8", "marketing_start_date": "20240108"}], "brand_name": "Prednisone", "product_id": "50090-7024_a94e9e6b-45f2-4e67-aef0-bf0256e10406", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "50090-7024", "generic_name": "Prednisone", "labeler_name": "A-S Medication Solutions", "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"}