NDC 0054-0017 – PredniSONE

Prednisone 10 mg/1 · Tablet · Oral

Human Prescription Drug 2 recalls

Product NDC0054-0017

Product details

Brand name
PredniSONE
Generic name
PredniSONE
Labeler
Hikma Pharmaceuticals USA Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA080352
Marketed since
February 13, 2003
Listing expires
December 31, 2026
Pharmacologic class
Corticosteroid

Active ingredients

Uses, dosage, side effects and warnings for Prednisone →

Package NDC codes (3)

Package NDCDescriptionSince
0054-0017-2010 BLISTER PACK in 1 CARTON (0054-0017-20) / 10 TABLET in 1 BLISTER PACKFeb 13, 2003
0054-0017-25100 TABLET in 1 BOTTLE, PLASTIC (0054-0017-25)Feb 13, 2003
0054-0017-29500 TABLET in 1 BOTTLE, PLASTIC (0054-0017-29)Feb 13, 2003

Recalls mentioning this NDC

Other Prednisone products