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0006-4305 NDC - RENFLEXIS ()

Drug Information

Product NDC: 0006-4305

Proprietary Name: Renflexis

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Merck Sharp & Dohme Corp.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:7/1/2017

Package Information

No. Package Code Package Description Billing Unit
10006-4305-021 VIAL in 1 CARTON (0006-4305-02) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (0006-4305-01)EA

NDC Record

Field Name Field Value Definition
PRODUCT NDC0006-4305The 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 NAMERenflexisThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE7/1/2017This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEMerck Sharp & Dohme Corp.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