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 5 mg/1

Manufacturer
QPharma, Inc.

Identifiers & Regulatory

Product NDC 42708-114
Product ID 42708-114_459c7779-af18-4654-e063-6294a90a9a2d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA080356
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 42708114
Hyphenated Format 42708-114

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 (source: ndc)
Generic Name prednisone (source: ndc)
Application Number ANDA080356 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 21 TABLET in 1 BOTTLE (42708-114-21)
source: ndc

Packages (1)

42708-114-21 21 TABLET in 1 BOTTLE (42708-114-21)

Ingredients (1)

prednisone (5 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": "459c7779-af18-4654-e063-6294a90a9a2d", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["VB0R961HZT"], "rxcui": ["312617"], "spl_set_id": ["f4d5974a-444f-4ef0-84a9-803150ccdeac"], "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 (42708-114-21)", "package_ndc": "42708-114-21", "marketing_start_date": "20180420"}], "brand_name": "Prednisone", "product_id": "42708-114_459c7779-af18-4654-e063-6294a90a9a2d", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "42708-114", "generic_name": "Prednisone", "labeler_name": "QPharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prednisone", "active_ingredients": [{"name": "PREDNISONE", "strength": "5 mg/1"}], "application_number": "ANDA080356", "marketing_category": "ANDA", "marketing_start_date": "19900101", "listing_expiration_date": "20261231"}