prednisone

Generic: prednisone

Labeler: major pharmaceuticals
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name prednisone
Generic Name prednisone
Labeler major pharmaceuticals
Dosage Form TABLET
Routes
ORAL
Active Ingredients

prednisone 10 mg/1

Manufacturer
Major Pharmaceuticals

Identifiers & Regulatory

Product NDC 0904-6923
Product ID 0904-6923_4eedc509-491a-40f4-b428-020497062d17
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040256
Listing Expiration 2026-12-31
Marketing Start 2002-07-12

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 09046923
Hyphenated Format 0904-6923

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 ANDA040256 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 CARTON (0904-6923-61) / 1 TABLET in 1 BLISTER PACK
source: ndc

Packages (1)

0904-6923-61 100 BLISTER PACK in 1 CARTON (0904-6923-61) / 1 TABLET in 1 BLISTER PACK

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": "4eedc509-491a-40f4-b428-020497062d17", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["VB0R961HZT"], "rxcui": ["198145"], "spl_set_id": ["57b98930-92ab-4b77-a033-ae9895ee718a"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-6923-61)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "0904-6923-61", "marketing_start_date": "20020712"}], "brand_name": "Prednisone", "product_id": "0904-6923_4eedc509-491a-40f4-b428-020497062d17", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "0904-6923", "generic_name": "Prednisone", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prednisone", "active_ingredients": [{"name": "PREDNISONE", "strength": "10 mg/1"}], "application_number": "ANDA040256", "marketing_category": "ANDA", "marketing_start_date": "20020712", "listing_expiration_date": "20261231"}