prednisone

Generic: prednisone

Labeler: preferred pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name prednisone
Generic Name prednisone
Labeler preferred pharmaceuticals inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

prednisone 20 mg/1

Manufacturer
Preferred Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 68788-8819
Product ID 68788-8819_94d82acb-ff31-492f-bd51-b23e15d881d6
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA215672
Listing Expiration 2026-12-31
Marketing Start 2025-01-23

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 687888819
Hyphenated Format 68788-8819

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 ANDA215672 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 10 TABLET in 1 BOTTLE (68788-8819-1)
  • 20 TABLET in 1 BOTTLE (68788-8819-2)
  • 30 TABLET in 1 BOTTLE (68788-8819-3)
  • 18 TABLET in 1 BOTTLE (68788-8819-4)
  • 15 TABLET in 1 BOTTLE (68788-8819-5)
  • 21 TABLET in 1 BOTTLE (68788-8819-8)
source: ndc

Packages (6)

68788-8819-1 10 TABLET in 1 BOTTLE (68788-8819-1) 68788-8819-2 20 TABLET in 1 BOTTLE (68788-8819-2) 68788-8819-3 30 TABLET in 1 BOTTLE (68788-8819-3) 68788-8819-4 18 TABLET in 1 BOTTLE (68788-8819-4) 68788-8819-5 15 TABLET in 1 BOTTLE (68788-8819-5) 68788-8819-8 21 TABLET in 1 BOTTLE (68788-8819-8)

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": "94d82acb-ff31-492f-bd51-b23e15d881d6", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["VB0R961HZT"], "rxcui": ["312615"], "spl_set_id": ["94d82acb-ff31-492f-bd51-b23e15d881d6"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET in 1 BOTTLE (68788-8819-1)", "package_ndc": "68788-8819-1", "marketing_start_date": "20250123"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (68788-8819-2)", "package_ndc": "68788-8819-2", "marketing_start_date": "20250123"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-8819-3)", "package_ndc": "68788-8819-3", "marketing_start_date": "20250123"}, {"sample": false, "description": "18 TABLET in 1 BOTTLE (68788-8819-4)", "package_ndc": "68788-8819-4", "marketing_start_date": "20250123"}, {"sample": false, "description": "15 TABLET in 1 BOTTLE (68788-8819-5)", "package_ndc": "68788-8819-5", "marketing_start_date": "20250123"}, {"sample": false, "description": "21 TABLET in 1 BOTTLE (68788-8819-8)", "package_ndc": "68788-8819-8", "marketing_start_date": "20250123"}], "brand_name": "PREDNISONE", "product_id": "68788-8819_94d82acb-ff31-492f-bd51-b23e15d881d6", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "68788-8819", "generic_name": "PREDNISONE", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PREDNISONE", "active_ingredients": [{"name": "PREDNISONE", "strength": "20 mg/1"}], "application_number": "ANDA215672", "marketing_category": "ANDA", "marketing_start_date": "20250123", "listing_expiration_date": "20261231"}