59883-912 NDC - PRO-DEN RX ()

Drug Information

Product NDC: 59883-912

Proprietary Name: Pro-Den Rx

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Den-mat Holdings, Llc
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:10/21/2008

Package Information

No. Package Code Package Description Billing Unit
159883-912-641890 mL in 1 BOTTLE, PLASTIC (59883-912-64)

NDC Record

Field Name Field Value Definition
PRODUCT NDC59883-912The 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 NAMEPro-Den RxThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE10/21/2008This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEDen-mat Holdings, LlcName 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