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 50090-1001
Product ID 50090-1001_513ab73a-aa62-4e74-a1e2-b4f6f878645e
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 500901001
Hyphenated Format 50090-1001

Supplemental Identifiers

RxCUI
198145 312615 763185
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
  • 21 TABLET in 1 BOX, UNIT-DOSE (50090-1001-0)
source: ndc

Packages (1)

50090-1001-0 21 TABLET in 1 BOX, UNIT-DOSE (50090-1001-0)

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": "513ab73a-aa62-4e74-a1e2-b4f6f878645e", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["VB0R961HZT"], "rxcui": ["198145", "312615", "763185"], "spl_set_id": ["b5b088b9-8f90-468f-b7a4-a5274aa0aec9"], "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 BOX, UNIT-DOSE (50090-1001-0)", "package_ndc": "50090-1001-0", "marketing_start_date": "20141128"}], "brand_name": "Prednisone", "product_id": "50090-1001_513ab73a-aa62-4e74-a1e2-b4f6f878645e", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "50090-1001", "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"}