70934-903 NDC - SILDENAFIL CITRATE ()

Drug Information

Product NDC: 70934-903

Proprietary Name: SILDENAFIL CITRATE

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Denton Pharma, Inc. DBA Northwind Pharmaceuticals
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:9/27/2021

Package Information

No. Package Code Package Description Billing Unit
170934-903-1515 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-903-15)

NDC Record

Field Name Field Value Definition
PRODUCT NDC70934-903The 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 NAMESILDENAFIL CITRATEThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE9/27/2021This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEDenton Pharma, Inc. DBA Northwind PharmaceuticalsName 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