66213-423 NDC - DONNATAL ()

Drug Information

Product NDC: 66213-423

Proprietary Name: Donnatal

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: PBM Pharmaceuticals Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:11/1/2009

Package Information

No. Package Code Package Description Billing Unit
166213-423-04118 mL in 1 BOTTLE (66213-423-04)ML
266213-423-16473 mL in 1 BOTTLE (66213-423-16)ML

NDC Record

Field Name Field Value Definition
PRODUCT NDC66213-423The 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 NAMEPBM Pharmaceuticals Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
PRODUCT NDC66213-423The 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 NAMEPBM Pharmaceuticals 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