prednisone intensol

Generic: prednisone intensol

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

Drug Facts

Product Profile

Brand Name prednisone intensol
Generic Name prednisone intensol
Labeler hikma pharmaceuticals usa inc.
Dosage Form SOLUTION, CONCENTRATE
Routes
ORAL
Active Ingredients

prednisone 5 mg/mL

Manufacturer
Hikma Pharmaceuticals USA Inc.

Identifiers & Regulatory

Product NDC 0054-3721
Product ID 0054-3721_523ad364-8d95-4679-9290-446d61f36eb5
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA088810
Listing Expiration 2026-12-31
Marketing Start 1985-02-20

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 00543721
Hyphenated Format 0054-3721

Supplemental Identifiers

RxCUI
198144 198145 198146 198148 205301 312615 312617 315187
UPC
0300543722507
UNII
VB0R961HZT
NUI
N0000175576 N0000175450

Packaging Origin

Original Packager
true

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 intensol (source: ndc)
Generic Name prednisone intensol (source: ndc)
Application Number ANDA088810 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/mL
source: ndc
Packaging
  • 30 mL in 1 BOTTLE, GLASS (0054-3721-44)
source: ndc

Packages (1)

0054-3721-44 30 mL in 1 BOTTLE, GLASS (0054-3721-44)

Ingredients (1)

prednisone (5 mg/mL)

Linked Drug Pages (1)

PredniSONE, PredniSONE Intensol ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "523ad364-8d95-4679-9290-446d61f36eb5", "openfda": {"nui": ["N0000175576", "N0000175450"], "upc": ["0300543722507"], "unii": ["VB0R961HZT"], "rxcui": ["198144", "198145", "198146", "198148", "205301", "312615", "312617", "315187"], "spl_set_id": ["3115aef0-fd50-4ec8-a064-3effb695f3f2"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 mL in 1 BOTTLE, GLASS (0054-3721-44)", "package_ndc": "0054-3721-44", "marketing_start_date": "19850220"}], "brand_name": "PredniSONE Intensol", "product_id": "0054-3721_523ad364-8d95-4679-9290-446d61f36eb5", "dosage_form": "SOLUTION, CONCENTRATE", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "0054-3721", "generic_name": "PredniSONE Intensol", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PredniSONE Intensol", "active_ingredients": [{"name": "PREDNISONE", "strength": "5 mg/mL"}], "application_number": "ANDA088810", "marketing_category": "ANDA", "marketing_start_date": "19850220", "listing_expiration_date": "20261231"}