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NDC 60505-0033-09 PENTOXIFYLLINE 400 mg/1 Details

PENTOXIFYLLINE 400 mg/1

PENTOXIFYLLINE is a ORAL TABLET, EXTENDED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Apotex Corp.. The primary component is PENTOXIFYLLINE.

MedlinePlus Drug Summary

Pentoxifylline is used to improve blood flow in patients with circulation problems to reduce aching, cramping, and tiredness in the hands and feet. It works by decreasing the thickness (viscosity) of blood. This change allows your blood to flow more easily, especially in the small blood vessels of the hands and feet. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.

Related Packages: 60505-0033-09
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Pentoxifylline

Product Information

NDC	60505-0033
Product ID	60505-0033_f96bc30c-f6a0-8913-979a-c65d53fa7bdc
Associated GPIs	85200010000410
GCN Sequence Number	006573
GCN Sequence Number Description	pentoxifylline TABLET ER 400 MG ORAL
HIC3	M9S
HIC3 Description	HEMORRHEOLOGIC AGENTS
GCN	11800
HICL Sequence Number	002819
HICL Sequence Number Description	PENTOXIFYLLINE
Brand/Generic	Generic
Proprietary Name	PENTOXIFYLLINE
Proprietary Name Suffix	n/a
Non-Proprietary Name	PENTOXIFYLLINE
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET, EXTENDED RELEASE
Route	ORAL
Active Ingredient Strength	400
Active Ingredient Units	mg/1
Substance Name	PENTOXIFYLLINE
Labeler Name	Apotex Corp.
Pharmaceutical Class	Blood Viscosity Reducer [EPC], Hematologic Activity Alteration [PE]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA075191
Listing Certified Through	2024-12-31

Package

NDC 60505-0033-09 (60505003309)

Pricing Information	N/A
NDC Package Code	60505-0033-9
Billing NDC	60505003309
Package	1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (60505-0033-9)
Marketing Start Date	1999-06-10
NDC Exclude Flag	N