68382-418 NDC - OXYMETAZOLINE HYDROCHLORIDE ()

Drug Information

Product NDC: 68382-418

Proprietary Name: OXYMETAZOLINE HYDROCHLORIDE

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Zydus Pharmaceuticals (USA) Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:9/24/2009

Package Information

No. Package Code Package Description Billing Unit
168382-418-071 INHALER in 1 CARTON (68382-418-07) / 22 mL in 1 INHALER

NDC Record

Field Name Field Value Definition
PRODUCT NDC68382-418The 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 HYDROCHLORIDEThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE9/24/2009This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEZydus Pharmaceuticals (USA) 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