17856-8100 NDC - SILDENAFIL CITRATE ()

Drug Information

Product NDC: 17856-8100

Proprietary Name: Sildenafil Citrate

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

No.	Package Code	Package Description
1	17856-8100-1	200 POUCH in 1 BOX (17856-8100-1) / 1 TABLET, FILM COATED in 1 POUCH
2	17856-8100-2	200 POUCH in 1 BOX (17856-8100-2) / 2 TABLET, FILM COATED in 1 POUCH
3	17856-8100-3	200 POUCH in 1 BOX (17856-8100-3) / 3 TABLET, FILM COATED in 1 POUCH
4	17856-8100-4	200 POUCH in 1 BOX (17856-8100-4) / 4 TABLET, FILM COATED in 1 POUCH
5	17856-8100-5	200 POUCH in 1 BOX (17856-8100-5) / 5 TABLET, FILM COATED in 1 POUCH

Field Name	Field Value	Definition
PRODUCT NDC	17856-8100	The 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 NAME	Sildenafil Citrate	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE	7/29/2019	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	ATLANTIC BIOLOGICALS CORP.	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