NDC 0603-5339 – Prednisone

Prednisone 20 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC0603-5339

Product details

Brand name
Prednisone
Generic name
Prednisone
Labeler
Par Health USA, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA040392
Marketed since
February 12, 2003
Listing expires
December 31, 2027
Pharmacologic class
Corticosteroid

Active ingredients

Uses, dosage, side effects and warnings for Prednisone →

Package NDC codes (3)

Package NDCDescriptionSince
0603-5339-21100 TABLET in 1 BOTTLE, PLASTIC (0603-5339-21)Feb 12, 2003
0603-5339-28500 TABLET in 1 BOTTLE, PLASTIC (0603-5339-28)Feb 12, 2003
0603-5339-321000 TABLET in 1 BOTTLE, PLASTIC (0603-5339-32)Feb 12, 2003

Recalls mentioning this NDC

Other Prednisone products