prednisone

Generic: prednisone

Labeler: redpharm drug
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

prednisone 20 mg/1

Manufacturer
Redpharm Drug

Identifiers & Regulatory

Product NDC 67296-2081
Product ID 67296-2081_46c1f121-0ec3-9a03-e063-6294a90acf7a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA213386
Listing Expiration 2026-12-31
Marketing Start 2020-06-24

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 672962081
Hyphenated Format 67296-2081

Supplemental Identifiers

RxCUI
312615
UPC
0360219170735 0360219170728 0360219170858 0360219170759
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 ANDA213386 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 10 TABLET in 1 BOTTLE (67296-2081-1)
  • 20 TABLET in 1 BOTTLE (67296-2081-2)
  • 15 TABLET in 1 BOTTLE (67296-2081-3)
  • 5 TABLET in 1 BOTTLE (67296-2081-5)
source: ndc

Packages (4)

Ingredients (1)

prednisone (20 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "46c1f121-0ec3-9a03-e063-6294a90acf7a", "openfda": {"nui": ["N0000175576", "N0000175450"], "upc": ["0360219170735", "0360219170728", "0360219170858", "0360219170759"], "unii": ["VB0R961HZT"], "rxcui": ["312615"], "spl_set_id": ["0ab0e81c-8170-6805-e063-6294a90adfc0"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["Redpharm Drug"]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET in 1 BOTTLE (67296-2081-1)", "package_ndc": "67296-2081-1", "marketing_start_date": "20200624"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (67296-2081-2)", "package_ndc": "67296-2081-2", "marketing_start_date": "20200624"}, {"sample": false, "description": "15 TABLET in 1 BOTTLE (67296-2081-3)", "package_ndc": "67296-2081-3", "marketing_start_date": "20200624"}, {"sample": false, "description": "5 TABLET in 1 BOTTLE (67296-2081-5)", "package_ndc": "67296-2081-5", "marketing_start_date": "20200624"}], "brand_name": "prednisone", "product_id": "67296-2081_46c1f121-0ec3-9a03-e063-6294a90acf7a", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "67296-2081", "generic_name": "prednisone", "labeler_name": "Redpharm Drug", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "prednisone", "active_ingredients": [{"name": "PREDNISONE", "strength": "20 mg/1"}], "application_number": "ANDA213386", "marketing_category": "ANDA", "marketing_start_date": "20200624", "listing_expiration_date": "20261231"}