41163-163 NDC - EQUALINE ()

Drug Information

Product NDC: 41163-163

Proprietary Name: EQUALINE

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: SUPERVALU INC.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:6/26/2012

Package Information

No. Package Code Package Description Billing Unit
141163-163-08221 mL in 1 BOTTLE, PUMP (41163-163-08)
241163-163-32946 mL in 1 BOTTLE, PLASTIC (41163-163-32)

NDC Record

Field Name Field Value Definition
PRODUCT NDC41163-163The 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 NAMEEQUALINEThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE7/2/2012This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMESUPERVALU INC.Name of Company corresponding to the labeler code segment of the Product NDC.
PRODUCT NDC41163-163The 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 NAMEEQUALINEThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE6/26/2012This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMESUPERVALU 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