NDC 64679-762 Midazolam Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 64679 - Wockhardt Usa Llc.
- 64679-762 - Midazolam Hydrochloride
Product Packages
NDC Code 64679-762-01
Package Description: 10 VIAL in 1 CARTON / 2 mL in 1 VIAL (64679-762-07)
NDC Code 64679-762-02
Package Description: 10 VIAL in 1 CARTON / 5 mL in 1 VIAL (64679-762-08)
NDC Code 64679-762-03
Package Description: 10 VIAL in 1 CARTON / 10 mL in 1 VIAL (64679-762-09)
NDC Code 64679-762-04
Package Description: 25 VIAL in 1 CARTON / 2 mL in 1 VIAL (64679-762-07)
NDC Code 64679-762-05
Package Description: 25 VIAL in 1 CARTON / 5 mL in 1 VIAL (64679-762-08)
NDC Code 64679-762-06
Package Description: 25 VIAL in 1 CARTON / 10 mL in 1 VIAL (64679-762-09)
Product Details
What is NDC 64679-762?
What are the uses for Midazolam Hydrochloride?
Which are Midazolam Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- MIDAZOLAM HYDROCHLORIDE (UNII: W7TTW573JJ)
- MIDAZOLAM (UNII: R60L0SM5BC) (Active Moiety)
Which are Midazolam Hydrochloride 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:
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- HYDROCHLORIC ACID (UNII: QTT17582CB)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
What is the NDC to RxNorm Crosswalk for Midazolam Hydrochloride?
- RxCUI: 311700 - midazolam 1 MG/ML Injectable Solution
- RxCUI: 311700 - midazolam (as midazolam hydrochloride) 1 MG/ML Injectable Solution
- RxCUI: 311702 - midazolam 5 MG/ML Injectable Solution
- RxCUI: 311702 - midazolam (as midazolam hydrochloride) 5 MG/ML Injectable Solution
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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".