NDC 70859-040 Point Of Care Lm 2.5
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 70859 - Nucare Pharmaceuticals,inc.
- 70859-040 - Point Of Care Lm 2.5
Product Packages
NDC Code 70859-040-01
Package Description: 1 KIT in 1 CARTON * 5 mL in 1 POUCH * 25 VIAL, SINGLE-DOSE in 1 CARTON (55150-167-10) / 10 mL in 1 VIAL, SINGLE-DOSE * 10 mL in 1 PACKET
Product Details
What is NDC 70859-040?
What are the uses for Point Of Care Lm 2.5?
Which are Point Of Care Lm 2.5 UNII Codes?
The UNII codes for the active ingredients in this product are:
- BUPIVACAINE HYDROCHLORIDE (UNII: 7TQO7W3VT8)
- BUPIVACAINE (UNII: Y8335394RO) (Active Moiety)
- POVIDONE-IODINE (UNII: 85H0HZU99M)
- IODINE (UNII: 9679TC07X4) (Active Moiety)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- ISOPROPYL ALCOHOL (UNII: ND2M416302) (Active Moiety)
Which are Point Of Care Lm 2.5 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:
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- WATER (UNII: 059QF0KO0R)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- HYDROCHLORIC ACID (UNII: QTT17582CB)
- SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
What is the NDC to RxNorm Crosswalk for Point Of Care Lm 2.5?
- RxCUI: 1725078 - BUPivacaine HCl 0.25 % in 10 ML Injection
- RxCUI: 1725078 - 10 ML bupivacaine hydrochloride 2.5 MG/ML Injection
- RxCUI: 1725078 - bupivacaine HCl 0.25 % in 10 ML Injection
- RxCUI: 797544 - isopropyl alcohol 70 % Medicated Pad
- RxCUI: 797544 - isopropyl alcohol 0.7 ML/ML Medicated Pad
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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".