NDC 51655-541 – prednisone

Prednisone 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC51655-541

Product details

Brand name
prednisone
Generic name
Prednisone
Labeler
Northwind Health Company, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA208412
Marketed since
May 19, 2023
Listing expires
December 31, 2027
Pharmacologic class
Corticosteroid

Active ingredients

Uses, dosage, side effects and warnings for Prednisone →

Package NDC codes (8)

Package NDCDescriptionSince
51655-541-1818 TABLET in 1 BOTTLE, PLASTIC (51655-541-18)Sep 4, 2025
51655-541-2020 TABLET in 1 BOTTLE, PLASTIC (51655-541-20)Dec 15, 2023
51655-541-2121 TABLET in 1 BOTTLE, PLASTIC (51655-541-21)Dec 28, 2023
51655-541-2712 TABLET in 1 BOTTLE, PLASTIC (51655-541-27)May 19, 2023
51655-541-5230 TABLET in 1 BOTTLE, PLASTIC (51655-541-52)Jul 12, 2023
51655-541-5310 TABLET in 1 BOTTLE, PLASTIC (51655-541-53)May 19, 2023
51655-541-5415 TABLET in 1 BOTTLE, PLASTIC (51655-541-54)Aug 15, 2023
51655-541-555 TABLET in 1 BOTTLE, PLASTIC (51655-541-55)Sep 30, 2025

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