NDC 0527-5406 – PrednisoLONE

Prednisolone 15 mg/5mL · Syrup · Oral

Human Prescription Drug

Product NDC0527-5406

Product details

Brand name
PrednisoLONE
Generic name
Prednisolone
Labeler
Lannett Company, Inc.
Dosage form
Syrup
Route
Oral
Marketing category
ANDA · ANDA040775
Marketed since
September 21, 2007
Listing expires
December 31, 2026
Pharmacologic class
Corticosteroid

Active ingredients

Uses, dosage, side effects and warnings for Prednisolone →

Package NDC codes (2)

Package NDCDescriptionSince
0527-5406-68240 mL in 1 BOTTLE (0527-5406-68)Sep 21, 2007
0527-5406-70480 mL in 1 BOTTLE (0527-5406-70)Sep 21, 2007

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