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68071-4532 NDC - PENTOXIFYLLINE ()

Drug Information

Product NDC: 68071-4532

Proprietary Name: Pentoxifylline

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: NuCare Pharmaceuticals,Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:8/22/2014

Package Information

No. Package Code Package Description Billing Unit
168071-4532-990 TABLET, EXTENDED RELEASE in 1 BOTTLE (68071-4532-9)

NDC Record

Field Name Field Value Definition
PRODUCT NDC68071-4532The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAMEPentoxifyllineThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE8/22/2014This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMENuCare Pharmaceuticals,Inc.Name of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 2/1/2023