prednisone

Generic: prednisone

Labeler: direct_rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name prednisone
Generic Name prednisone
Labeler direct_rx
Dosage Form TABLET
Routes
ORAL
Active Ingredients

prednisone 50 mg/1

Manufacturer
Direct_Rx

Identifiers & Regulatory

Product NDC 72189-489
Product ID 72189-489_2c4e30d6-25ee-5c75-e063-6294a90a2fc2
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA208412
Listing Expiration 2026-12-31
Marketing Start 2023-06-07

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 72189489
Hyphenated Format 72189-489

Supplemental Identifiers

RxCUI
198148
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 ANDA208412 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 7 TABLET in 1 BOTTLE (72189-489-07)
source: ndc

Packages (1)

72189-489-07 7 TABLET in 1 BOTTLE (72189-489-07)

Ingredients (1)

prednisone (50 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": "2c4e30d6-25ee-5c75-e063-6294a90a2fc2", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["VB0R961HZT"], "rxcui": ["198148"], "spl_set_id": ["fd8eb82e-52df-c368-e053-6294a90ac6b0"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "7 TABLET in 1 BOTTLE (72189-489-07)", "package_ndc": "72189-489-07", "marketing_start_date": "20230607"}], "brand_name": "Prednisone", "product_id": "72189-489_2c4e30d6-25ee-5c75-e063-6294a90a2fc2", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "72189-489", "generic_name": "Prednisone", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prednisone", "active_ingredients": [{"name": "PREDNISONE", "strength": "50 mg/1"}], "application_number": "ANDA208412", "marketing_category": "ANDA", "marketing_start_date": "20230607", "listing_expiration_date": "20261231"}