55312-111 NDC - WESTERN FAMILY ()

Drug Information

Product NDC: 55312-111

Proprietary Name: Western Family

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Name:	WESTERN FAMILY HOLDING COMPANY
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:	12/16/2013

No.	Package Code	Package Description	Billing Unit
1	55312-111-11	1 BOTTLE in 1 CARTON (55312-111-11) / 133 mL in 1 BOTTLE
2	55312-111-35	2 BOTTLE in 1 CARTON (55312-111-35) / 133 mL in 1 BOTTLE

Field Name	Field Value	Definition
PRODUCT NDC	55312-111	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	Western Family	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	12/16/2013	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	WESTERN FAMILY HOLDING COMPANY	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