24338-080 NDC - OTOVEL ()

Drug Information

Product NDC: 24338-080

Proprietary Name: OTOVEL

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Arbor Pharmaceuticals
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:4/29/2016

Package Information

No. Package Code Package Description Billing Unit
124338-080-141 POUCH in 1 CARTON (24338-080-14) / 14 VIAL, SINGLE-DOSE in 1 POUCH / .25 mL in 1 VIAL, SINGLE-DOSE (24338-080-25)

NDC Record

Field Name Field Value Definition
PRODUCT NDC24338-080The 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 NAMEOTOVELThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE4/29/2016This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEArbor 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