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PREDNISONE

NDC 87063-045 · ASCLEMED USA INC.

Generic namePREDNISONE
Dosage formTABLET
RouteORAL
Active ingredient(s)PREDNISONE
Strength20 mg/1
Pharmacologic classCorticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
Marketing categoryANDA

Packages

87063-045-01 100 TABLET in 1 BOTTLE (87063-045-01)

87063-045-18 18 TABLET in 1 BOTTLE (87063-045-18)

87063-045-20 20 TABLET in 1 BOTTLE (87063-045-20)

87063-045-21 21 TABLET in 1 BOTTLE (87063-045-21)

87063-045-30 30 TABLET in 1 BOTTLE (87063-045-30)

87063-045-60 60 TABLET in 1 BOTTLE (87063-045-60)

87063-045-78 10 BLISTER PACK in 1 CARTON (87063-045-78) / 10 TABLET in 1 BLISTER PACK

87063-045-90 90 TABLET in 1 BOTTLE (87063-045-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

80425-0106 — Prednisone, 80425-0193 — Prednisone, 80425-0479 — PREDNISONE, 80425-0480 — PredniSONE, 80425-0481 — PredniSONE, 80425-0482 — PREDNISONE, 80425-0484 — PREDNISONE, 80425-0485 — PredniSONE, 80425-0486 — Prednisone, 80425-0487 — PREDNISONE, 80425-0491 — Prednisone, 82804-223 — Prednisone, 85766-001 — PREDNISONE, 85766-002 — PREDNISONE, 85766-086 — PREDNISONE, 87063-042 — PREDNISONE, 87063-043 — PREDNISONE, 87063-044 — PREDNISONE, 87063-048 — PREDNISONE, 87441-069 — prednisone, +288 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.