NDC 70529-010 Acunistat-30
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 70529 - It3 Medical Llc
- 70529-010 - Acunistat-30
Product Packages
NDC Code 70529-010-01
Package Description: 1 KIT in 1 PACKAGE * 1 mL in 1 VIAL, SINGLE-DOSE * 1 mL in 1 PACKET * 50 mL in 1 VIAL, MULTI-DOSE
Product Details
What is NDC 70529-010?
What are the uses for Acunistat-30?
Which are Acunistat-30 UNII Codes?
The UNII codes for the active ingredients in this product are:
- LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A)
- LIDOCAINE (UNII: 98PI200987) (Active Moiety)
- KETOROLAC TROMETHAMINE (UNII: 4EVE5946BQ)
- KETOROLAC (UNII: YZI5105V0L) (Active Moiety)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- ISOPROPYL ALCOHOL (UNII: ND2M416302) (Active Moiety)
Which are Acunistat-30 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 CHLORIDE (UNII: 451W47IQ8X)
- WATER (UNII: 059QF0KO0R)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- HYDROCHLORIC ACID (UNII: QTT17582CB)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- ALCOHOL (UNII: 3K9958V90M)
What is the NDC to RxNorm Crosswalk for Acunistat-30?
- RxCUI: 1010033 - lidocaine HCl 1 % Injectable Solution
- RxCUI: 1010033 - lidocaine hydrochloride 10 MG/ML Injectable Solution
- RxCUI: 1010033 - lidocaine hydrochloride 1 % Injectable Solution
- RxCUI: 1665461 - ketorolac tromethamine 30 MG in 1 ML Injection
- RxCUI: 1665461 - 1 ML ketorolac tromethamine 30 MG/ML Injection
* Please review the disclaimer below.
[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".