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 55289-330
Product ID 55289-330_419e633a-5422-21c2-e063-6394a90a9634
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA084283
Listing Expiration 2026-12-31
Marketing Start 2003-02-13

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 55289330
Hyphenated Format 55289-330

Supplemental Identifiers

RxCUI
198145
UPC
0355289330059
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 ANDA084283 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 5 TABLET in 1 BOTTLE, PLASTIC (55289-330-05)
  • 7 TABLET in 1 BOTTLE, PLASTIC (55289-330-07)
  • 10 TABLET in 1 BOTTLE, PLASTIC (55289-330-10)
source: ndc

Packages (3)

55289-330-05 5 TABLET in 1 BOTTLE, PLASTIC (55289-330-05) 55289-330-07 7 TABLET in 1 BOTTLE, PLASTIC (55289-330-07) 55289-330-10 10 TABLET in 1 BOTTLE, PLASTIC (55289-330-10)

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": "419e633a-5422-21c2-e063-6394a90a9634", "openfda": {"nui": ["N0000175576", "N0000175450"], "upc": ["0355289330059"], "unii": ["VB0R961HZT"], "rxcui": ["198145"], "spl_set_id": ["5b2f4fa9-817c-43c9-ac9a-750ab1d1f66f"], "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": "5 TABLET in 1 BOTTLE, PLASTIC (55289-330-05)", "package_ndc": "55289-330-05", "marketing_start_date": "20091118"}, {"sample": false, "description": "7 TABLET in 1 BOTTLE, PLASTIC (55289-330-07)", "package_ndc": "55289-330-07", "marketing_start_date": "20091118"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE, PLASTIC (55289-330-10)", "package_ndc": "55289-330-10", "marketing_start_date": "20091118"}], "brand_name": "PredniSONE", "product_id": "55289-330_419e633a-5422-21c2-e063-6394a90a9634", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "55289-330", "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": "ANDA084283", "marketing_category": "ANDA", "marketing_start_date": "20030213", "listing_expiration_date": "20261231"}