NDC 0603-5337 – Prednisone

Prednisone 5 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC0603-5337

Product details

Brand name
Prednisone
Generic name
Prednisone
Labeler
Par Health USA, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA040256
Marketed since
July 12, 2002
Listing expires
December 31, 2027
Pharmacologic class
Corticosteroid

Active ingredients

Uses, dosage, side effects and warnings for Prednisone →

Package NDC codes (4)

Package NDCDescriptionSince
0603-5337-1521 TABLET in 1 BOX, UNIT-DOSE (0603-5337-15)Jul 12, 2002
0603-5337-21100 TABLET in 1 BOTTLE, PLASTIC (0603-5337-21)Jul 12, 2002
0603-5337-3148 TABLET in 1 BOX, UNIT-DOSE (0603-5337-31)Jul 12, 2002
0603-5337-321000 TABLET in 1 BOTTLE, PLASTIC (0603-5337-32)Jul 12, 2002

Recalls mentioning this NDC

Other Prednisone products