NDC 70529-007 Durapren 0.75%
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What is NDC 70529-007?
What are the uses for Durapren 0.75%?
Which are Durapren 0.75% UNII Codes?
The UNII codes for the active ingredients in this product are:
- BUPIVACAINE HYDROCHLORIDE (UNII: 7TQO7W3VT8)
- BUPIVACAINE (UNII: Y8335394RO) (Active Moiety)
Which are Durapren 0.75% 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)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- HYDROCHLORIC ACID (UNII: QTT17582CB)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Durapren 0.75%?
- RxCUI: 1724786 - BUPivacaine HCl 0.75 % in 30 ML Injection
- RxCUI: 1724786 - 30 ML bupivacaine hydrochloride 7.5 MG/ML Injection
- RxCUI: 1724786 - bupivacaine HCl 0.75 % in 30 ML Injection
- RxCUI: 1724786 - bupivacaine HCl 225 MG per 30 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".