49348-864 NDC - SUNMARK ()

Drug Information

Product NDC: 49348-864

Proprietary Name: Sunmark

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Mckesson Corporation
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:3/6/2013

Package Information

No. Package Code Package Description Billing Unit
149348-864-142 BOTTLE in 1 CARTON (49348-864-14) / 133 mL in 1 BOTTLEML
249348-864-201 BOTTLE in 1 CARTON (49348-864-20) / 133 mL in 1 BOTTLEML

NDC Record

Field Name Field Value Definition
PRODUCT NDC49348-864The 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 NAMESunmarkThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE3/6/2013This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEMckesson CorporationName 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