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 50 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-6225
Product ID 50090-6225_52fbc187-4c61-4081-bd30-67636c407009
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211575
Listing Expiration 2026-12-31
Marketing Start 2019-11-15

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 500906225
Hyphenated Format 50090-6225

Supplemental Identifiers

RxCUI
198148
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 ANDA211575 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 8 TABLET in 1 BOTTLE (50090-6225-0)
source: ndc

Packages (1)

50090-6225-0 8 TABLET in 1 BOTTLE (50090-6225-0)

Ingredients (1)

prednisone (50 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": "52fbc187-4c61-4081-bd30-67636c407009", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["VB0R961HZT"], "rxcui": ["198148"], "spl_set_id": ["8f7a38c7-7bf9-4951-b529-947cc9a57d6a"], "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": "8 TABLET in 1 BOTTLE (50090-6225-0)", "package_ndc": "50090-6225-0", "marketing_start_date": "20221114"}], "brand_name": "Prednisone", "product_id": "50090-6225_52fbc187-4c61-4081-bd30-67636c407009", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "50090-6225", "generic_name": "Prednisone", "labeler_name": "A-S Medication Solutions", "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": "20191115", "listing_expiration_date": "20261231"}