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17089-281 NDC - GUNA-TF PAPILLOMA ()

Drug Information

Product NDC: 17089-281

Proprietary Name: GUNA-TF PAPILLOMA

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Guna spa
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:4/16/2008

Package Information

No. Package Code Package Description Billing Unit
117089-281-101 BOTTLE in 1 BOX (17089-281-10) / 4600 mg in 1 BOTTLE

NDC Record

Field Name Field Value Definition
PRODUCT NDC17089-281The 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 NAMEGUNA-TF PAPILLOMAThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE4/16/2008This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEGuna spaName 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