NDC 69938-153 Disposable Convenience Kit (single Shot Epidural)
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 69938-153?
What are the uses for Disposable Convenience Kit (single Shot Epidural)?
Which are Disposable Convenience Kit (single Shot Epidural) UNII Codes?
The UNII codes for the active ingredients in this product are:
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- CHLORIDE ION (UNII: Q32ZN48698) (Active Moiety)
- POVIDONE-IODINE (UNII: 85H0HZU99M)
- IODINE (UNII: 9679TC07X4) (Active Moiety)
- BUPIVACAINE HYDROCHLORIDE (UNII: 7TQO7W3VT8)
- BUPIVACAINE (UNII: Y8335394RO) (Active Moiety)
- LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A)
- LIDOCAINE (UNII: 98PI200987) (Active Moiety)
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:
- WATER (UNII: 059QF0KO0R)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74)
- NONOXYNOL-9 (UNII: 48Q180SH9T)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- HYDROCHLORIC ACID (UNII: QTT17582CB)
What is the NDC to RxNorm Crosswalk for Disposable Convenience Kit (single Shot Epidural)?
- RxCUI: 1010033 - lidocaine HCl 1 % Injectable Solution
- RxCUI: 1010033 - lidocaine hydrochloride 10 MG/ML Injectable Solution
- RxCUI: 1010033 - lidocaine hydrochloride 1 % Injectable Solution
- RxCUI: 1725082 - BUPivacaine HCl 0.25 % in 30 ML Injection
- RxCUI: 1725082 - 30 ML bupivacaine hydrochloride 2.5 MG/ML Injection
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[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".