prednisone

Generic: prednisone

Labeler: northwind health company, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name prednisone
Generic Name prednisone
Labeler northwind health company, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

prednisone 20 mg/1

Manufacturer
Northwind Health Company, LLC

Identifiers & Regulatory

Product NDC 51655-701
Product ID 51655-701_4950ead0-97a4-b291-e063-6294a90a6026
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA087342
Listing Expiration 2027-12-31
Marketing Start 2021-04-19

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 51655701
Hyphenated Format 51655-701

Supplemental Identifiers

RxCUI
312615
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 ANDA087342 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 18 TABLET in 1 BOTTLE, PLASTIC (51655-701-18)
  • 20 TABLET in 1 BOTTLE, PLASTIC (51655-701-20)
  • 10 TABLET in 1 BOTTLE, PLASTIC (51655-701-53)
source: ndc

Packages (3)

51655-701-18 18 TABLET in 1 BOTTLE, PLASTIC (51655-701-18) 51655-701-20 20 TABLET in 1 BOTTLE, PLASTIC (51655-701-20) 51655-701-53 10 TABLET in 1 BOTTLE, PLASTIC (51655-701-53)

Ingredients (1)

prednisone (20 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": "4950ead0-97a4-b291-e063-6294a90a6026", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["VB0R961HZT"], "rxcui": ["312615"], "spl_set_id": ["ca39fdfb-d110-6535-e053-2995a90a550a"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "18 TABLET in 1 BOTTLE, PLASTIC (51655-701-18)", "package_ndc": "51655-701-18", "marketing_start_date": "20210610"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE, PLASTIC (51655-701-20)", "package_ndc": "51655-701-20", "marketing_start_date": "20210610"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE, PLASTIC (51655-701-53)", "package_ndc": "51655-701-53", "marketing_start_date": "20210419"}], "brand_name": "PredniSONE", "product_id": "51655-701_4950ead0-97a4-b291-e063-6294a90a6026", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "51655-701", "generic_name": "PredniSONE", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PredniSONE", "active_ingredients": [{"name": "PREDNISONE", "strength": "20 mg/1"}], "application_number": "ANDA087342", "marketing_category": "ANDA", "marketing_start_date": "20210419", "listing_expiration_date": "20271231"}