17856-0423 NDC - DONNATAL ()

Drug Information

Product NDC: 17856-0423

Proprietary Name: Donnatal

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Atlantic Biologicals Corps
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:11/1/2009

Package Information

No. Package Code Package Description Billing Unit
117856-0423-215 mL in 1 CUP (17856-0423-2)
217856-0423-310 mL in 1 CUP (17856-0423-3)ML
317856-0423-45 mL in 1 CUP (17856-0423-4)
417856-0423-55 mL in 1 CUP (17856-0423-5)ML
517856-0423-610 CUP in 1 CASE (17856-0423-6) / 5 mL in 1 CUP
617856-0423-815 mL in 1 CUP (17856-0423-8)
717856-0423-910 mL in 1 CUP (17856-0423-9)

NDC Record

Field Name Field Value Definition
PRODUCT NDC17856-0423The 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 NAMEDonnatalThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE11/1/2009This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEAtlantic Biologicals CorpsName 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