PENTOXIFYLLINE

NDC 0904-5448 · Major Pharmaceuticals

Generic namePENTOXIFYLLINE

Dosage formTABLET, EXTENDED RELEASE

RouteORAL

Active ingredient(s)PENTOXIFYLLINE

Strength400 mg/1

Pharmacologic classBlood Viscosity Reducer [EPC], Hematologic Activity Alteration [PE]

Marketing categoryANDA

Packages

0904-5448-61 — 100 BLISTER PACK in 1 CARTON (0904-5448-61) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

FDA lists these products with the same active ingredient.

0615-8511 — Pentoxifylline, 16571-856 — Pentoxifylline, 60505-0033 — PENTOXIFYLLINE, 63629-2910 — PENTOXIFYLLINE, 70954-668 — Pentoxifylline, 71335-2586 — Pentoxifylline

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.