prednisone

Generic: prednisone

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name prednisone
Generic Name prednisone
Labeler proficient rx lp
Dosage Form TABLET
Routes
ORAL
Active Ingredients

prednisone 20 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-407
Product ID 71205-407_e100760e-78a5-42b1-9efb-52a5680737fa
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211575
Listing Expiration 2026-12-31
Marketing Start 2019-11-15

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 71205407
Hyphenated Format 71205-407

Supplemental Identifiers

RxCUI
312615
UPC
0371205407155
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 ANDA211575 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 10 TABLET in 1 BOTTLE (71205-407-10)
  • 15 TABLET in 1 BOTTLE (71205-407-15)
  • 18 TABLET in 1 BOTTLE (71205-407-18)
  • 20 TABLET in 1 BOTTLE (71205-407-20)
  • 21 TABLET in 1 BOTTLE (71205-407-21)
  • 30 TABLET in 1 BOTTLE (71205-407-30)
  • 60 TABLET in 1 BOTTLE (71205-407-60)
  • 90 TABLET in 1 BOTTLE (71205-407-90)
source: ndc

Packages (8)

71205-407-10 10 TABLET in 1 BOTTLE (71205-407-10) 71205-407-15 15 TABLET in 1 BOTTLE (71205-407-15) 71205-407-18 18 TABLET in 1 BOTTLE (71205-407-18) 71205-407-20 20 TABLET in 1 BOTTLE (71205-407-20) 71205-407-21 21 TABLET in 1 BOTTLE (71205-407-21) 71205-407-30 30 TABLET in 1 BOTTLE (71205-407-30) 71205-407-60 60 TABLET in 1 BOTTLE (71205-407-60) 71205-407-90 90 TABLET in 1 BOTTLE (71205-407-90)

Ingredients (1)

prednisone (20 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": "e100760e-78a5-42b1-9efb-52a5680737fa", "openfda": {"nui": ["N0000175576", "N0000175450"], "upc": ["0371205407155"], "unii": ["VB0R961HZT"], "rxcui": ["312615"], "spl_set_id": ["67681e4e-3002-4428-af5e-6ff1a950b037"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET in 1 BOTTLE (71205-407-10)", "package_ndc": "71205-407-10", "marketing_start_date": "20200219"}, {"sample": false, "description": "15 TABLET in 1 BOTTLE (71205-407-15)", "package_ndc": "71205-407-15", "marketing_start_date": "20200403"}, {"sample": false, "description": "18 TABLET in 1 BOTTLE (71205-407-18)", "package_ndc": "71205-407-18", "marketing_start_date": "20200519"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (71205-407-20)", "package_ndc": "71205-407-20", "marketing_start_date": "20200219"}, {"sample": false, "description": "21 TABLET in 1 BOTTLE (71205-407-21)", "package_ndc": "71205-407-21", "marketing_start_date": "20200219"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (71205-407-30)", "package_ndc": "71205-407-30", "marketing_start_date": "20200219"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71205-407-60)", "package_ndc": "71205-407-60", "marketing_start_date": "20200219"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71205-407-90)", "package_ndc": "71205-407-90", "marketing_start_date": "20200219"}], "brand_name": "Prednisone", "product_id": "71205-407_e100760e-78a5-42b1-9efb-52a5680737fa", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "71205-407", "generic_name": "Prednisone", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prednisone", "active_ingredients": [{"name": "PREDNISONE", "strength": "20 mg/1"}], "application_number": "ANDA211575", "marketing_category": "ANDA", "marketing_start_date": "20191115", "listing_expiration_date": "20261231"}