NDC 64679-661 Granisetron Hydrochloride
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What is NDC 64679-661?
Which are Granisetron Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- GRANISETRON HYDROCHLORIDE (UNII: 318F6L70J8)
- GRANISETRON (UNII: WZG3J2MCOL) (Active Moiety)
Which are Granisetron 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:
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- HYDROCHLORIC ACID (UNII: QTT17582CB)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Granisetron Hydrochloride?
- RxCUI: 1734399 - granisetron HCl 1 MG in 1 ML Injection
- RxCUI: 1734399 - 1 ML granisetron 1 MG/ML Injection
- RxCUI: 1734399 - granisetron 1 MG (as granisetron HCl 1.12 MG) per 1 ML Injection
- RxCUI: 1734399 - granisetron 1 MG per 1 ML Injection
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Patient Education
Granisetron Injection
Granisetron immediate-release injection is used to prevent nausea and vomiting caused by cancer chemotherapy and to prevent and treat nausea and vomiting that may occur after surgery. Granisetron extended-release (long-acting) injection is used with other medications to prevent nausea and vomiting caused by cancer chemotherapy that may occur immediately or several days after receiving chemotherapy medications. Granisetron is in a class of medications called 5-HT3 receptor antagonists. It works by blocking serotonin, a natural substance in the body that causes nausea and vomiting.
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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".