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Prednisone

NDC 71205-089 · Proficient Rx LP

Generic namePrednisone
Dosage formTABLET
RouteORAL
Active ingredient(s)PREDNISONE
Strength1 mg/1
Pharmacologic classCorticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
Marketing categoryANDA

Packages

71205-089-00 100 TABLET in 1 BOTTLE (71205-089-00)

71205-089-05 5 TABLET in 1 BOTTLE (71205-089-05)

71205-089-06 6 TABLET in 1 BOTTLE (71205-089-06)

71205-089-07 7 TABLET in 1 BOTTLE (71205-089-07)

71205-089-08 8 TABLET in 1 BOTTLE (71205-089-08)

71205-089-10 10 TABLET in 1 BOTTLE (71205-089-10)

71205-089-12 12 TABLET in 1 BOTTLE (71205-089-12)

71205-089-15 15 TABLET in 1 BOTTLE (71205-089-15)

71205-089-18 18 TABLET in 1 BOTTLE (71205-089-18)

71205-089-20 20 TABLET in 1 BOTTLE (71205-089-20)

71205-089-21 21 TABLET in 1 BOTTLE (71205-089-21)

71205-089-24 24 TABLET in 1 BOTTLE (71205-089-24)

71205-089-27 27 TABLET in 1 BOTTLE (71205-089-27)

71205-089-30 30 TABLET in 1 BOTTLE (71205-089-30)

71205-089-36 36 TABLET in 1 BOTTLE (71205-089-36)

71205-089-40 40 TABLET in 1 BOTTLE (71205-089-40)

71205-089-42 42 TABLET in 1 BOTTLE (71205-089-42)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70518-4293 — PREDNISONE, 70518-4354 — prednisone, 70518-4560 — PREDNISONE, 70518-4660 — PREDNISONE, 70954-056 — Prednisone, 70954-057 — Prednisone, 70954-058 — Prednisone, 70954-059 — Prednisone, 70954-060 — Prednisone, 70954-061 — Prednisone, 71205-239 — Prednisone, 71205-362 — Prednisone, 71205-407 — Prednisone, 71205-421 — Prednisone, 71205-665 — Prednisone, 71205-729 — PREDNISONE, 71205-741 — PREDNISONE, 71205-755 — PREDNISONE, 71205-797 — prednisone, 71205-818 — 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.