70655-002 NDC - FLUCONAZOLE IN SODIUM CHLORIDE ()

Drug Information

Product NDC: 70655-002

Proprietary Name: Fluconazole in Sodium Chloride

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Renaissance SSA, LLC
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:9/12/2018

Package Information

No. Package Code Package Description Billing Unit
170655-002-066 BAG in 1 CARTON (70655-002-06) / 100 mL in 1 BAGML
270655-002-1010 BAG in 1 CARTON (70655-002-10) / 100 mL in 1 BAGML

NDC Record

Field Name Field Value Definition
PRODUCT NDC70655-002The 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 NAMEFluconazole in Sodium ChlorideThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE9/12/2018This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMERenaissance SSA, LLCName 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