NDC 68788-8663 – Prednisone

Prednisone 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68788-8663

Product details

Brand name
Prednisone
Generic name
Prednisone
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA208412
Marketed since
May 13, 2024
Listing expires
December 31, 2027
Pharmacologic class
Corticosteroid

Active ingredients

Uses, dosage, side effects and warnings for Prednisone →

Package NDC codes (6)

Package NDCDescriptionSince
68788-8663-110 TABLET in 1 BOTTLE, PLASTIC (68788-8663-1)May 13, 2024
68788-8663-220 TABLET in 1 BOTTLE, PLASTIC (68788-8663-2)May 13, 2024
68788-8663-330 TABLET in 1 BOTTLE, PLASTIC (68788-8663-3)May 13, 2024
68788-8663-418 TABLET in 1 BOTTLE, PLASTIC (68788-8663-4)May 13, 2024
68788-8663-515 TABLET in 1 BOTTLE, PLASTIC (68788-8663-5)May 13, 2024
68788-8663-821 TABLET in 1 BOTTLE, PLASTIC (68788-8663-8)May 13, 2024

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