NDC 51655-701 – PredniSONE

Prednisone 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC51655-701

Product details

Brand name
PredniSONE
Generic name
PredniSONE
Labeler
Northwind Health Company, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA087342
Marketed since
April 19, 2021
Listing expires
December 31, 2027
Pharmacologic class
Corticosteroid

Active ingredients

Uses, dosage, side effects and warnings for Prednisone →

Package NDC codes (3)

Package NDCDescriptionSince
51655-701-1818 TABLET in 1 BOTTLE, PLASTIC (51655-701-18)Jun 10, 2021
51655-701-2020 TABLET in 1 BOTTLE, PLASTIC (51655-701-20)Jun 10, 2021
51655-701-5310 TABLET in 1 BOTTLE, PLASTIC (51655-701-53)Apr 19, 2021

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