61699-4888 NDC - SODIUM CHLORIDE ()

Drug Information

Product NDC: 61699-4888

Proprietary Name: Sodium Chloride

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: US MedSource, LLC
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:6/19/2014

Package Information

No. Package Code Package Description Billing Unit
161699-4888-11 VIAL, SINGLE-DOSE in 1 BAG (61699-4888-1) / 10 mL in 1 VIAL, SINGLE-DOSE

NDC Record

Field Name Field Value Definition
PRODUCT NDC61699-4888The 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 NAMESodium 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 DATE6/19/2014This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEUS MedSource, 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