NDC 0641-6032 Flumazenil
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 0641 - West-ward Pharmaceutical Corp.
- 0641-6032 - Flumazenil
Product Packages
NDC Code 0641-6032-10
Package Description: 10 VIAL in 1 CARTON / 10 mL in 1 VIAL (0641-6032-01)
Product Details
What is NDC 0641-6032?
What are the uses for Flumazenil?
Which are Flumazenil UNII Codes?
The UNII codes for the active ingredients in this product are:
- FLUMAZENIL (UNII: 40P7XK9392)
- FLUMAZENIL (UNII: 40P7XK9392) (Active Moiety)
Which are Flumazenil 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:
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- ACETIC ACID (UNII: Q40Q9N063P)
- HYDROCHLORIC ACID (UNII: QTT17582CB)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Flumazenil?
- RxCUI: 204508 - flumazenil 0.1 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".