NDC 60219-1708 – Prednisone

Prednisone 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC60219-1708

Product details

Brand name
Prednisone
Generic name
Prednisone
Labeler
Amneal Pharmaceuticals NY LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA213386
Marketed since
June 24, 2020
Listing expires
December 31, 2027
Pharmacologic class
Corticosteroid

Active ingredients

Uses, dosage, side effects and warnings for Prednisone →

Package NDC codes (2)

Package NDCDescriptionSince
60219-1708-1100 TABLET in 1 BOTTLE, PLASTIC (60219-1708-1)Jun 24, 2020
60219-1708-5500 TABLET in 1 BOTTLE, PLASTIC (60219-1708-5)Jun 24, 2020

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