Pentoxifylline
NDC 16571-856 · Rising Pharma Holdings, Inc.
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
16571-856-01 — 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (16571-856-01)
16571-856-05 — 50 BLISTER PACK in 1 CARTON (16571-856-05) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
16571-856-11 — 10 BLISTER PACK in 1 CARTON (16571-856-11) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
16571-856-50 — 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (16571-856-50)
16571-856-90 — 1 BLISTER PACK in 1 CARTON (16571-856-90) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Related Codes
Same active ingredient
FDA lists these products with the same active ingredient.
0615-8511 — Pentoxifylline, 0904-5448 — PENTOXIFYLLINE, 60505-0033 — PENTOXIFYLLINE, 63629-2910 — PENTOXIFYLLINE, 70954-668 — Pentoxifylline, 71335-2586 — Pentoxifylline