NDC 60722-5011 – Prednisolone

Prednisolone 5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC60722-5011

Product details

Brand name
Prednisolone
Generic name
Prednisolone
Labeler
Zhejiang Xianju Pharmaceutical Co., Ltd.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA218083
Marketed since
September 1, 2024
Listing expires
December 31, 2027
Pharmacologic class
Corticosteroid

Active ingredients

Uses, dosage, side effects and warnings for Prednisolone →

Package NDC codes (2)

Package NDCDescriptionSince
60722-5011-0100 TABLET in 1 BOTTLE (60722-5011-0)Sep 1, 2024
60722-5011-11000 TABLET in 1 BOTTLE (60722-5011-1)Sep 1, 2024

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