prednisone

Generic: prednisone

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name prednisone
Generic Name prednisone
Labeler pd-rx pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

prednisone 10 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72789-401
Product ID 72789-401_2e815bd0-baeb-9631-e063-6394a90a49c8
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 72789401
Hyphenated Format 72789-401

Supplemental Identifiers

RxCUI
198145
UPC
0372789401300
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
  • 10 mg/1
source: ndc
Packaging
  • 10 TABLET in 1 BOTTLE, PLASTIC (72789-401-10)
  • 12 TABLET in 1 BOTTLE, PLASTIC (72789-401-12)
  • 20 TABLET in 1 BOTTLE, PLASTIC (72789-401-20)
  • 21 TABLET in 1 BOTTLE, PLASTIC (72789-401-21)
  • 30 TABLET in 1 BOTTLE, PLASTIC (72789-401-30)
  • 40 TABLET in 1 BOTTLE, PLASTIC (72789-401-40)
  • 42 TABLET in 1 BOTTLE, PLASTIC (72789-401-42)
  • 50 TABLET in 1 BOTTLE, PLASTIC (72789-401-50)
source: ndc

Packages (8)

72789-401-10 10 TABLET in 1 BOTTLE, PLASTIC (72789-401-10) 72789-401-12 12 TABLET in 1 BOTTLE, PLASTIC (72789-401-12) 72789-401-20 20 TABLET in 1 BOTTLE, PLASTIC (72789-401-20) 72789-401-21 21 TABLET in 1 BOTTLE, PLASTIC (72789-401-21) 72789-401-30 30 TABLET in 1 BOTTLE, PLASTIC (72789-401-30) 72789-401-40 40 TABLET in 1 BOTTLE, PLASTIC (72789-401-40) 72789-401-42 42 TABLET in 1 BOTTLE, PLASTIC (72789-401-42) 72789-401-50 50 TABLET in 1 BOTTLE, PLASTIC (72789-401-50)

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": "2e815bd0-baeb-9631-e063-6394a90a49c8", "openfda": {"nui": ["N0000175576", "N0000175450"], "upc": ["0372789401300"], "unii": ["VB0R961HZT"], "rxcui": ["198145"], "spl_set_id": ["19fdbf9f-3a64-b9fa-e063-6394a90af086"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET in 1 BOTTLE, PLASTIC (72789-401-10)", "package_ndc": "72789-401-10", "marketing_start_date": "20240604"}, {"sample": false, "description": "12 TABLET in 1 BOTTLE, PLASTIC (72789-401-12)", "package_ndc": "72789-401-12", "marketing_start_date": "20240710"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE, PLASTIC (72789-401-20)", "package_ndc": "72789-401-20", "marketing_start_date": "20240620"}, {"sample": false, "description": "21 TABLET in 1 BOTTLE, PLASTIC (72789-401-21)", "package_ndc": "72789-401-21", "marketing_start_date": "20240625"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (72789-401-30)", "package_ndc": "72789-401-30", "marketing_start_date": "20240603"}, {"sample": false, "description": "40 TABLET in 1 BOTTLE, PLASTIC (72789-401-40)", "package_ndc": "72789-401-40", "marketing_start_date": "20240603"}, {"sample": false, "description": "42 TABLET in 1 BOTTLE, PLASTIC (72789-401-42)", "package_ndc": "72789-401-42", "marketing_start_date": "20250110"}, {"sample": false, "description": "50 TABLET in 1 BOTTLE, PLASTIC (72789-401-50)", "package_ndc": "72789-401-50", "marketing_start_date": "20240603"}], "brand_name": "Prednisone", "product_id": "72789-401_2e815bd0-baeb-9631-e063-6394a90a49c8", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "72789-401", "generic_name": "Prednisone", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prednisone", "active_ingredients": [{"name": "PREDNISONE", "strength": "10 mg/1"}], "application_number": "ANDA211575", "marketing_category": "ANDA", "marketing_start_date": "20191115", "listing_expiration_date": "20261231"}