66213-421 NDC - DONNATAL EXTENTABS ()

Drug Information

Product NDC: 66213-421

Proprietary Name: Donnatal Extentabs

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:5/7/2008

Package Information

No. Package Code Package Description Billing Unit
166213-421-10100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (66213-421-10)EA
266213-421-50500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (66213-421-50)EA

NDC Record

Field Name Field Value Definition
PRODUCT NDC66213-421The 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 NAMEDonnatal ExtentabsThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE5/7/2008This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEPBM Pharmaceuticals, IncName 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