50436-0035 NDC - SILDENAFIL CITRATE ()

Drug Information

Product NDC: 50436-0035

Proprietary Name: Sildenafil Citrate

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Unit Dose Services
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:12/1/2017

Package Information

No. Package Code Package Description Billing Unit
150436-0035-1200 POUCH in 1 CASE (50436-0035-1) / 1 TABLET, FILM COATED in 1 POUCH

NDC Record

Field Name Field Value Definition
PRODUCT NDC50436-0035The 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 DATE12/1/2017This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEUnit Dose ServicesName 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