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prednisone

NDC 71205-755 · Proficient Rx LP

Generic namePREDNISONE
Dosage formTABLET
RouteORAL
Active ingredient(s)PREDNISONE
Strength50 mg/1
Pharmacologic classCorticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
Marketing categoryANDA

Packages

71205-755-05 5 TABLET in 1 BOTTLE (71205-755-05)

71205-755-06 6 TABLET in 1 BOTTLE (71205-755-06)

71205-755-07 7 TABLET in 1 BOTTLE (71205-755-07)

71205-755-10 10 TABLET in 1 BOTTLE (71205-755-10)

71205-755-12 12 TABLET in 1 BOTTLE (71205-755-12)

71205-755-14 14 TABLET in 1 BOTTLE (71205-755-14)

71205-755-15 15 TABLET in 1 BOTTLE (71205-755-15)

71205-755-18 18 TABLET in 1 BOTTLE (71205-755-18)

71205-755-20 20 TABLET in 1 BOTTLE (71205-755-20)

71205-755-21 21 TABLET in 1 BOTTLE (71205-755-21)

71205-755-24 24 TABLET in 1 BOTTLE (71205-755-24)

71205-755-28 28 TABLET in 1 BOTTLE (71205-755-28)

71205-755-30 30 TABLET in 1 BOTTLE (71205-755-30)

71205-755-60 60 TABLET in 1 BOTTLE (71205-755-60)

71205-755-90 90 TABLET in 1 BOTTLE (71205-755-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70954-060 — Prednisone, 70954-061 — Prednisone, 71205-089 — Prednisone, 71205-239 — Prednisone, 71205-362 — Prednisone, 71205-407 — Prednisone, 71205-421 — Prednisone, 71205-665 — Prednisone, 71205-729 — PREDNISONE, 71205-741 — PREDNISONE, 71205-797 — prednisone, 71205-818 — prednisone, 71335-1780 — Prednisone, 71335-2069 — PREDNISONE, 71335-2079 — PREDNISONE, 71335-2088 — PREDNISONE, 71335-2122 — PREDNISONE, 71335-2134 — PREDNISONE, 71335-2149 — PREDNISONE, 71335-2160 — 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.