NDC 72789-473 – PredniSONE Tablets, USP, 20 mg

Prednisone 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC72789-473

Product details

Brand name
PredniSONE Tablets, USP, 20 mg
Generic name
PredniSONE
Labeler
PD-Rx Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA212629
Marketed since
May 22, 2025
Listing expires
December 31, 2027
Pharmacologic class
Corticosteroid

Active ingredients

Uses, dosage, side effects and warnings for PredniSONE Tablets, USP, 20 mg →

Package NDC codes (12)

Package NDCDescriptionSince
72789-473-01100 TABLET in 1 BOTTLE, PLASTIC (72789-473-01)May 22, 2025
72789-473-044 TABLET in 1 BOTTLE, PLASTIC (72789-473-04)Dec 24, 2025
72789-473-055 TABLET in 1 BOTTLE, PLASTIC (72789-473-05)Jun 9, 2025
72789-473-1010 TABLET in 1 BOTTLE, PLASTIC (72789-473-10)Jun 10, 2025
72789-473-1414 TABLET in 1 BOTTLE, PLASTIC (72789-473-14)Mar 4, 2026
72789-473-1515 TABLET in 1 BOTTLE, PLASTIC (72789-473-15)Aug 21, 2026
72789-473-1818 TABLET in 1 BOTTLE, PLASTIC (72789-473-18)Apr 6, 2026
72789-473-2020 TABLET in 1 BOTTLE, PLASTIC (72789-473-20)Jun 9, 2025
72789-473-2121 TABLET in 1 BOTTLE, PLASTIC (72789-473-21)May 22, 2025
72789-473-2525 TABLET in 1 BOTTLE, PLASTIC (72789-473-25)May 22, 2025
72789-473-3030 TABLET in 1 BOTTLE, PLASTIC (72789-473-30)May 30, 2025
72789-473-951000 TABLET in 1 BOTTLE, PLASTIC (72789-473-95)May 22, 2025

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