76413-335 NDC - DIABETIC TUSSIN EXPECTORANT ()

Drug Information

Product NDC: 76413-335

Proprietary Name: Diabetic Tussin Expectorant

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Name:	Central Texas Community Health Centers
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:	1/1/1996

No.	Package Code	Package Description	Billing Unit
1	76413-335-01	118 mL in 1 BOTTLE (76413-335-01)

Field Name	Field Value	Definition
PRODUCT NDC	76413-335	The 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 NAME	Diabetic Tussin Expectorant	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE	1/1/1996	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	Central Texas Community Health Centers	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