NDC 71335-2586 – Pentoxifylline

Pentoxifylline 400 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug

Product NDC71335-2586

Product details

Brand name
Pentoxifylline
Generic name
Pentoxifylline
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA074425
Marketed since
June 11, 2024
Listing expires
December 31, 2026
Pharmacologic class
Blood Viscosity Reducer

Active ingredients

Uses, dosage, side effects and warnings for Pentoxifylline →

Package NDC codes (3)

Package NDCDescriptionSince
71335-2586-130 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2586-1)Apr 7, 2025
71335-2586-260 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2586-2)Apr 7, 2025
71335-2586-390 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2586-3)Apr 7, 2025

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