prednisone

Generic: prednisone

Labeler: atlantic biologicals corps
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name prednisone
Generic Name prednisone
Labeler atlantic biologicals corps
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

prednisone 5 mg/5mL

Manufacturer
Atlantic Biologicals Corps

Identifiers & Regulatory

Product NDC 17856-3722
Product ID 17856-3722_35d2e5c3-3d05-e219-e063-6294a90acf21
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA088703
Listing Expiration 2026-12-31
Marketing Start 1986-12-13

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 178563722
Hyphenated Format 17856-3722

Supplemental Identifiers

RxCUI
315187
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 ANDA088703 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/5mL
source: ndc
Packaging
  • 5 mL in 1 CUP (17856-3722-1)
source: ndc

Packages (1)

17856-3722-1 5 mL in 1 CUP (17856-3722-1)

Ingredients (1)

prednisone (5 mg/5mL)

Linked Drug Pages (1)

PredniSONE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "35d2e5c3-3d05-e219-e063-6294a90acf21", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["VB0R961HZT"], "rxcui": ["315187"], "spl_set_id": ["07be390e-ef1e-4bf9-a9da-4338b5f6cfa5"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["Atlantic Biologicals Corps"]}, "finished": true, "packaging": [{"sample": false, "description": "5 mL in 1 CUP (17856-3722-1)", "package_ndc": "17856-3722-1", "marketing_start_date": "20160505"}], "brand_name": "PredniSONE", "product_id": "17856-3722_35d2e5c3-3d05-e219-e063-6294a90acf21", "dosage_form": "SOLUTION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "17856-3722", "generic_name": "PredniSONE", "labeler_name": "Atlantic Biologicals Corps", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PredniSONE", "active_ingredients": [{"name": "PREDNISONE", "strength": "5 mg/5mL"}], "application_number": "ANDA088703", "marketing_category": "ANDA", "marketing_start_date": "19861213", "listing_expiration_date": "20261231"}