NDC 67877-184 Granisetron Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 67877 - Ascend Laboratories, Llc
- 67877-184 - Granisetron Hydrochloride
Product Characteristics
Product Packages
NDC Code 67877-184-02
Package Description: 2 TABLET in 1 BLISTER PACK
Price per Unit: $3.78764 per EA
NDC Code 67877-184-20
Package Description: 20 TABLET in 1 BLISTER PACK
Price per Unit: $3.78764 per EA
Product Details
What is NDC 67877-184?
What are the uses for Granisetron Hydrochloride?
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:
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- POLYETHYLENE GLYCOL 4000 (UNII: 4R4HFI6D95)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Granisetron Hydrochloride?
- RxCUI: 310599 - granisetron HCl 1 MG Oral Tablet
- RxCUI: 310599 - granisetron 1 MG Oral Tablet
- RxCUI: 310599 - granisetron 1 MG (granisetron hydrochloride 1.12 MG) Oral Tablet
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Patient Education
Granisetron
Granisetron is used to prevent nausea and vomiting caused by cancer chemotherapy and radiation therapy. 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".