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 20 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 43063-703
Product ID 43063-703_3ed98dc5-52ff-b876-e063-6394a90afd12
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040362
Marketing Start 2001-08-29
Marketing End 2026-05-01

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 43063703
Hyphenated Format 43063-703

Supplemental Identifiers

RxCUI
312615
UPC
0343063703304
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 ANDA040362 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 5 TABLET in 1 BOTTLE, PLASTIC (43063-703-05)
  • 6 TABLET in 1 BOTTLE, PLASTIC (43063-703-06)
  • 9 TABLET in 1 BOTTLE, PLASTIC (43063-703-09)
  • 10 TABLET in 1 BOTTLE, PLASTIC (43063-703-10)
  • 12 TABLET in 1 BOTTLE, PLASTIC (43063-703-12)
  • 14 TABLET in 1 BOTTLE, PLASTIC (43063-703-14)
  • 15 TABLET in 1 BOTTLE, PLASTIC (43063-703-15)
  • 18 TABLET in 1 BOTTLE, PLASTIC (43063-703-18)
  • 20 TABLET in 1 BOTTLE, PLASTIC (43063-703-20)
  • 21 TABLET in 1 BOTTLE, PLASTIC (43063-703-21)
  • 25 TABLET in 1 BOTTLE, PLASTIC (43063-703-25)
  • 30 TABLET in 1 BOTTLE, PLASTIC (43063-703-30)
source: ndc

Packages (12)

Ingredients (1)

prednisone (20 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3ed98dc5-52ff-b876-e063-6394a90afd12", "openfda": {"nui": ["N0000175576", "N0000175450"], "upc": ["0343063703304"], "unii": ["VB0R961HZT"], "rxcui": ["312615"], "spl_set_id": ["8dc46c79-d5a6-4203-84cd-9644334e7653"], "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 (43063-703-05)", "package_ndc": "43063-703-05", "marketing_end_date": "20260501", "marketing_start_date": "20161117"}, {"sample": false, "description": "6 TABLET in 1 BOTTLE, PLASTIC (43063-703-06)", "package_ndc": "43063-703-06", "marketing_end_date": "20260501", "marketing_start_date": "20161003"}, {"sample": false, "description": "9 TABLET in 1 BOTTLE, PLASTIC (43063-703-09)", "package_ndc": "43063-703-09", "marketing_end_date": "20260501", "marketing_start_date": "20160915"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE, PLASTIC (43063-703-10)", "package_ndc": "43063-703-10", "marketing_end_date": "20260501", "marketing_start_date": "20010829"}, {"sample": false, "description": "12 TABLET in 1 BOTTLE, PLASTIC (43063-703-12)", "package_ndc": "43063-703-12", "marketing_end_date": "20260501", "marketing_start_date": "20161107"}, {"sample": false, "description": "14 TABLET in 1 BOTTLE, PLASTIC (43063-703-14)", "package_ndc": "43063-703-14", "marketing_end_date": "20260501", "marketing_start_date": "20161107"}, {"sample": false, "description": "15 TABLET in 1 BOTTLE, PLASTIC (43063-703-15)", "package_ndc": "43063-703-15", "marketing_end_date": "20260501", "marketing_start_date": "20160914"}, {"sample": false, "description": "18 TABLET in 1 BOTTLE, PLASTIC (43063-703-18)", "package_ndc": "43063-703-18", "marketing_end_date": "20260501", "marketing_start_date": "20160817"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE, PLASTIC (43063-703-20)", "package_ndc": "43063-703-20", "marketing_end_date": "20260501", "marketing_start_date": "20160822"}, {"sample": false, "description": "21 TABLET in 1 BOTTLE, PLASTIC (43063-703-21)", "package_ndc": "43063-703-21", "marketing_end_date": "20260501", "marketing_start_date": "20160817"}, {"sample": false, "description": "25 TABLET in 1 BOTTLE, PLASTIC (43063-703-25)", "package_ndc": "43063-703-25", "marketing_end_date": "20260501", "marketing_start_date": "20160208"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (43063-703-30)", "package_ndc": "43063-703-30", "marketing_end_date": "20260501", "marketing_start_date": "20160822"}], "brand_name": "Prednisone", "product_id": "43063-703_3ed98dc5-52ff-b876-e063-6394a90afd12", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "43063-703", "generic_name": "Prednisone", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prednisone", "active_ingredients": [{"name": "PREDNISONE", "strength": "20 mg/1"}], "application_number": "ANDA040362", "marketing_category": "ANDA", "marketing_end_date": "20260501", "marketing_start_date": "20010829"}