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 20 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-6122
Product ID 50090-6122_4466f506-8a9b-4e9d-ac63-f3e9af2bac4c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA213386
Listing Expiration 2026-12-31
Marketing Start 2020-06-24

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 500906122
Hyphenated Format 50090-6122

Supplemental Identifiers

RxCUI
312615
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 ANDA213386 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 10 TABLET in 1 BOTTLE (50090-6122-1)
  • 21 TABLET in 1 BOTTLE (50090-6122-2)
  • 30 TABLET in 1 BOTTLE (50090-6122-3)
  • 100 TABLET in 1 BOTTLE (50090-6122-5)
  • 18 TABLET in 1 BOTTLE (50090-6122-9)
source: ndc

Packages (5)

50090-6122-1 10 TABLET in 1 BOTTLE (50090-6122-1) 50090-6122-2 21 TABLET in 1 BOTTLE (50090-6122-2) 50090-6122-3 30 TABLET in 1 BOTTLE (50090-6122-3) 50090-6122-5 100 TABLET in 1 BOTTLE (50090-6122-5) 50090-6122-9 18 TABLET in 1 BOTTLE (50090-6122-9)

Ingredients (1)

prednisone (20 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": "4466f506-8a9b-4e9d-ac63-f3e9af2bac4c", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["VB0R961HZT"], "rxcui": ["312615"], "spl_set_id": ["8f9a581c-5fef-4089-aa94-7dc81ec5b566"], "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 (50090-6122-1)", "package_ndc": "50090-6122-1", "marketing_start_date": "20220930"}, {"sample": false, "description": "21 TABLET in 1 BOTTLE (50090-6122-2)", "package_ndc": "50090-6122-2", "marketing_start_date": "20220930"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-6122-3)", "package_ndc": "50090-6122-3", "marketing_start_date": "20220930"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (50090-6122-5)", "package_ndc": "50090-6122-5", "marketing_start_date": "20220930"}, {"sample": false, "description": "18 TABLET in 1 BOTTLE (50090-6122-9)", "package_ndc": "50090-6122-9", "marketing_start_date": "20220930"}], "brand_name": "prednisone", "product_id": "50090-6122_4466f506-8a9b-4e9d-ac63-f3e9af2bac4c", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "50090-6122", "generic_name": "prednisone", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "prednisone", "active_ingredients": [{"name": "PREDNISONE", "strength": "20 mg/1"}], "application_number": "ANDA213386", "marketing_category": "ANDA", "marketing_start_date": "20200624", "listing_expiration_date": "20261231"}