73414-002 NDC - OXYMETAZOLINE HCL ()

Drug Information

Product NDC: 73414-002

Proprietary Name: OXYMETAZOLINE HCl

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Seaway Pharma Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:1/1/2020

Package Information

No. Package Code Package Description Billing Unit
173414-002-021 BOTTLE in 1 CARTON (73414-002-02) / 30 mL in 1 BOTTLE
273414-002-171 BOTTLE in 1 CARTON (73414-002-17) / 15 mL in 1 BOTTLE

NDC Record

Field Name Field Value Definition
PRODUCT NDC73414-002The 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 NAMEOXYMETAZOLINE HClThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE1/1/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMESeaway Pharma Inc.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