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 50 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72789-426
Product ID 72789-426_4123bf5c-0b1e-3307-e063-6294a90aa6b6
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA215672
Listing Expiration 2026-12-31
Marketing Start 2022-03-28

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 72789426
Hyphenated Format 72789-426

Supplemental Identifiers

RxCUI
198148
UPC
0372789426051
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 ANDA215672 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 5 TABLET in 1 BOTTLE, PLASTIC (72789-426-05)
source: ndc

Packages (1)

72789-426-05 5 TABLET in 1 BOTTLE, PLASTIC (72789-426-05)

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": "4123bf5c-0b1e-3307-e063-6294a90aa6b6", "openfda": {"nui": ["N0000175576", "N0000175450"], "upc": ["0372789426051"], "unii": ["VB0R961HZT"], "rxcui": ["198148"], "spl_set_id": ["c21be016-6b25-4e09-b253-23b58884ccb6"], "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 (72789-426-05)", "package_ndc": "72789-426-05", "marketing_start_date": "20240812"}], "brand_name": "PREDNISONE", "product_id": "72789-426_4123bf5c-0b1e-3307-e063-6294a90aa6b6", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "72789-426", "generic_name": "PREDNISONE", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PREDNISONE", "active_ingredients": [{"name": "PREDNISONE", "strength": "50 mg/1"}], "application_number": "ANDA215672", "marketing_category": "ANDA", "marketing_start_date": "20220328", "listing_expiration_date": "20261231"}