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 5 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-6619
Product ID 50090-6619_6866c32d-8ecf-41b3-846f-d0cb9f820a26
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA080352
Listing Expiration 2026-12-31
Marketing Start 2020-03-23

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 500906619
Hyphenated Format 50090-6619

Supplemental Identifiers

RxCUI
312617
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 ANDA080352 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 21 TABLET in 1 BOTTLE (50090-6619-0)
  • 50 TABLET in 1 BOTTLE (50090-6619-1)
  • 100 TABLET in 1 BOTTLE (50090-6619-3)
  • 30 TABLET in 1 BOTTLE (50090-6619-4)
  • 60 TABLET in 1 BOTTLE (50090-6619-7)
source: ndc

Packages (5)

50090-6619-0 21 TABLET in 1 BOTTLE (50090-6619-0) 50090-6619-1 50 TABLET in 1 BOTTLE (50090-6619-1) 50090-6619-3 100 TABLET in 1 BOTTLE (50090-6619-3) 50090-6619-4 30 TABLET in 1 BOTTLE (50090-6619-4) 50090-6619-7 60 TABLET in 1 BOTTLE (50090-6619-7)

Ingredients (1)

prednisone (5 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": "6866c32d-8ecf-41b3-846f-d0cb9f820a26", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["VB0R961HZT"], "rxcui": ["312617"], "spl_set_id": ["f11c190e-edf8-454d-82c4-1ed769b5a6d2"], "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": "21 TABLET in 1 BOTTLE (50090-6619-0)", "package_ndc": "50090-6619-0", "marketing_start_date": "20230824"}, {"sample": false, "description": "50 TABLET in 1 BOTTLE (50090-6619-1)", "package_ndc": "50090-6619-1", "marketing_start_date": "20230824"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (50090-6619-3)", "package_ndc": "50090-6619-3", "marketing_start_date": "20230824"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-6619-4)", "package_ndc": "50090-6619-4", "marketing_start_date": "20230824"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (50090-6619-7)", "package_ndc": "50090-6619-7", "marketing_start_date": "20230824"}], "brand_name": "PredniSONE", "product_id": "50090-6619_6866c32d-8ecf-41b3-846f-d0cb9f820a26", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "50090-6619", "generic_name": "PredniSONE", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PredniSONE", "active_ingredients": [{"name": "PREDNISONE", "strength": "5 mg/1"}], "application_number": "ANDA080352", "marketing_category": "ANDA", "marketing_start_date": "20200323", "listing_expiration_date": "20261231"}