prednisone

Generic: prednisone

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

Drug Facts

Product Profile

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

prednisone 10 mg/1

Manufacturer
Hikma Pharmaceuticals USA Inc.

Identifiers & Regulatory

Product NDC 0054-9817
Product ID 0054-9817_249c4c6d-a058-489a-8f84-928c14bfd3f9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA080352
Listing Expiration 2026-12-31
Marketing Start 2020-03-23

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 00549817
Hyphenated Format 0054-9817

Supplemental Identifiers

RxCUI
198145 312615 312617
UPC
0300549817252 0300549828258 0300549818259
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 (source: ndc)
Generic Name prednisone (source: ndc)
Application Number ANDA080352 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (0054-9817-25)
  • 500 TABLET in 1 BOTTLE (0054-9817-29)
source: ndc

Packages (2)

0054-9817-25 100 TABLET in 1 BOTTLE (0054-9817-25) 0054-9817-29 500 TABLET in 1 BOTTLE (0054-9817-29)

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": "249c4c6d-a058-489a-8f84-928c14bfd3f9", "openfda": {"nui": ["N0000175576", "N0000175450"], "upc": ["0300549817252", "0300549828258", "0300549818259"], "unii": ["VB0R961HZT"], "rxcui": ["198145", "312615", "312617"], "spl_set_id": ["263ed4fa-3c29-4abb-9cb1-bc016bd34a05"], "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": "100 TABLET in 1 BOTTLE (0054-9817-25)", "package_ndc": "0054-9817-25", "marketing_start_date": "20200323"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (0054-9817-29)", "package_ndc": "0054-9817-29", "marketing_start_date": "20200323"}], "brand_name": "PredniSONE", "product_id": "0054-9817_249c4c6d-a058-489a-8f84-928c14bfd3f9", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "0054-9817", "generic_name": "PredniSONE", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PredniSONE", "active_ingredients": [{"name": "PREDNISONE", "strength": "10 mg/1"}], "application_number": "ANDA080352", "marketing_category": "ANDA", "marketing_start_date": "20200323", "listing_expiration_date": "20261231"}