Pentoxifylline

Product NDC

51079-889

11-digit product format

510790889

Labeler code

51079

Product ID

51079-889_7d7c9caf-523a-f8c3-e053-2a91aa0a7aa1

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Pentoxifylline

Dosage form

TABLET, FILM COATED, EXTENDED RELEASE

Route

ORAL

Labeler

Mylan Institutional Inc.

Application

ANDA074425

Marketing category

ANDA

Marketing start

1998-01-15

Marketing end

2019-05-31

Substance

PENTOXIFYLLINE

Active strength

400 mg/1

Pharmacologic classes

Blood Viscosity Reducer [EPC],Hematologic Activity Alteration [PE]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record