prednisone

Generic: prednisone

Labeler: qpharma, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name prednisone
Generic Name prednisone
Labeler qpharma, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

prednisone 10 mg/1

Manufacturer
QPharma, Inc.

Identifiers & Regulatory

Product NDC 42708-115
Product ID 42708-115_459c17d6-14bb-9d87-e063-6294a90af969
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA085162
Listing Expiration 2026-12-31
Marketing Start 1990-01-01

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 42708115
Hyphenated Format 42708-115

Supplemental Identifiers

RxCUI
198145
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 ANDA085162 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 21 TABLET in 1 BOTTLE (42708-115-21)
source: ndc

Packages (1)

42708-115-21 21 TABLET in 1 BOTTLE (42708-115-21)

Ingredients (1)

prednisone (10 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": "459c17d6-14bb-9d87-e063-6294a90af969", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["VB0R961HZT"], "rxcui": ["198145"], "spl_set_id": ["07fb8daa-2ceb-4564-b0d0-6cdf903da0b5"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["QPharma, Inc."]}, "finished": true, "packaging": [{"sample": true, "description": "21 TABLET in 1 BOTTLE (42708-115-21)", "package_ndc": "42708-115-21", "marketing_start_date": "20180420"}], "brand_name": "Prednisone", "product_id": "42708-115_459c17d6-14bb-9d87-e063-6294a90af969", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "42708-115", "generic_name": "Prednisone", "labeler_name": "QPharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prednisone", "active_ingredients": [{"name": "PREDNISONE", "strength": "10 mg/1"}], "application_number": "ANDA085162", "marketing_category": "ANDA", "marketing_start_date": "19900101", "listing_expiration_date": "20261231"}