prednisone tablets, usp, 20 mg

Generic: prednisone

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name prednisone tablets, usp, 20 mg
Generic Name prednisone
Labeler pd-rx pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

prednisone 20 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72789-509
Product ID 72789-509_3ac67c26-d570-32a9-e063-6294a90a1048
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA212629
Listing Expiration 2026-12-31
Marketing Start 2025-05-22

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 72789509
Hyphenated Format 72789-509

Supplemental Identifiers

RxCUI
312615
UPC
0372789509150
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 tablets, usp, 20 mg (source: ndc)
Generic Name prednisone (source: ndc)
Application Number ANDA212629 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 6 TABLET in 1 BOTTLE, PLASTIC (72789-509-06)
  • 9 TABLET in 1 BOTTLE, PLASTIC (72789-509-09)
  • 12 TABLET in 1 BOTTLE, PLASTIC (72789-509-12)
  • 15 TABLET in 1 BOTTLE, PLASTIC (72789-509-15)
source: ndc

Packages (4)

72789-509-06 6 TABLET in 1 BOTTLE, PLASTIC (72789-509-06) 72789-509-09 9 TABLET in 1 BOTTLE, PLASTIC (72789-509-09) 72789-509-12 12 TABLET in 1 BOTTLE, PLASTIC (72789-509-12) 72789-509-15 15 TABLET in 1 BOTTLE, PLASTIC (72789-509-15)

Ingredients (1)

prednisone (20 mg/1)

Linked Drug Pages (1)

PredniSONE Tablets, USP, 20 mg ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3ac67c26-d570-32a9-e063-6294a90a1048", "openfda": {"nui": ["N0000175576", "N0000175450"], "upc": ["0372789509150"], "unii": ["VB0R961HZT"], "rxcui": ["312615"], "spl_set_id": ["15230866-f547-47bf-ac7d-19afd6a41e2e"], "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": "6 TABLET in 1 BOTTLE, PLASTIC (72789-509-06)", "package_ndc": "72789-509-06", "marketing_start_date": "20250620"}, {"sample": false, "description": "9 TABLET in 1 BOTTLE, PLASTIC (72789-509-09)", "package_ndc": "72789-509-09", "marketing_start_date": "20250527"}, {"sample": false, "description": "12 TABLET in 1 BOTTLE, PLASTIC (72789-509-12)", "package_ndc": "72789-509-12", "marketing_start_date": "20250709"}, {"sample": false, "description": "15 TABLET in 1 BOTTLE, PLASTIC (72789-509-15)", "package_ndc": "72789-509-15", "marketing_start_date": "20250522"}], "brand_name": "PredniSONE Tablets, USP, 20 mg", "product_id": "72789-509_3ac67c26-d570-32a9-e063-6294a90a1048", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "72789-509", "generic_name": "PredniSONE", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PredniSONE Tablets, USP, 20 mg", "active_ingredients": [{"name": "PREDNISONE", "strength": "20 mg/1"}], "application_number": "ANDA212629", "marketing_category": "ANDA", "marketing_start_date": "20250522", "listing_expiration_date": "20261231"}