NDC 69938-153 Disposable Convenience Kit (single Shot Epidural)

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
69938-153
Proprietary Name:
Disposable Convenience Kit (single Shot Epidural)
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Labeler Code:
69938
Start Marketing Date: [9]
02-04-2016
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Characteristics

Code Structure Chart

Product Details

What is NDC 69938-153?

The NDC code 69938-153 is assigned by the FDA to the product Disposable Convenience Kit (single Shot Epidural) which is product labeled by True Fit Rx Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69938-153-21 1 kit in 1 kit * 22.5 ml in 1 packet * 30 ml in 1 ampule * 5 ml in 1 ampule * 1 ampule in 1 kit / 10 ml in 1 ampule. This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Disposable Convenience Kit (single Shot Epidural)?

Sodium Chloride Injection is used to flush intravascular catheters or as a sterile, isotonic single dose vehicle, solvent, or diluent for substances to be administered intravenously, intramuscularly or subcutaneously and for other extemporaneously prepared single dose sterile solutions according to instructions of the manufacture of the drug to be administered.

Which are Disposable Convenience Kit (single Shot Epidural) UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Disposable Convenience Kit (single Shot Epidural) Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

What is the NDC to RxNorm Crosswalk for Disposable Convenience Kit (single Shot Epidural)?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

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Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".