prednisone tablets, usp, 5 mg

Generic: prednisone

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name prednisone tablets, usp, 5 mg
Generic Name prednisone
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

prednisone 5 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-3042
Product ID 71335-3042_f7d09338-d177-49e0-8b2c-f4f794312e4c
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 713353042
Hyphenated Format 71335-3042

Supplemental Identifiers

RxCUI
312617
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, 5 mg (source: ndc)
Generic Name prednisone (source: ndc)
Application Number ANDA212629 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (71335-3042-1)
source: ndc

Packages (1)

71335-3042-1 100 TABLET in 1 BOTTLE (71335-3042-1)

Ingredients (1)

prednisone (5 mg/1)

Linked Drug Pages (1)

PredniSONE Tablets, USP, 5 mg ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "f7d09338-d177-49e0-8b2c-f4f794312e4c", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["VB0R961HZT"], "rxcui": ["312617"], "spl_set_id": ["5e5c81bf-7cbb-4f02-b107-16efe3d353ee"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-3042-1)", "package_ndc": "71335-3042-1", "marketing_start_date": "20251203"}], "brand_name": "PredniSONE Tablets, USP, 5 mg", "product_id": "71335-3042_f7d09338-d177-49e0-8b2c-f4f794312e4c", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "71335-3042", "generic_name": "PredniSONE", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PredniSONE Tablets, USP, 5 mg", "active_ingredients": [{"name": "PREDNISONE", "strength": "5 mg/1"}], "application_number": "ANDA212629", "marketing_category": "ANDA", "marketing_start_date": "20250522", "listing_expiration_date": "20261231"}