NDC 51672-4110 Ondansetron Hydrochloride
Tablet, Film Coated Oral - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 51672 - Taro Pharmaceuticals U.s.a., Inc.
- 51672-4110 - Ondansetron Hydrochloride
Product Characteristics
WHITE (C48325)
PINK (C48328)
13 MM
TARO;OND8
TARO;OND24
Product Packages
NDC Code 51672-4110-5
Package Description: 1 BLISTER PACK in 1 CARTON / 1 TABLET, FILM COATED in 1 BLISTER PACK
Product Details
What is NDC 51672-4110?
What are the uses for Ondansetron Hydrochloride?
What are Ondansetron Hydrochloride Active Ingredients?
- ONDANSETRON HYDROCHLORIDE 24 mg/1 - A competitive serotonin type 3 receptor antagonist. It is effective in the treatment of nausea and vomiting caused by cytotoxic chemotherapy drugs, including cisplatin, and has reported anxiolytic and neuroleptic properties.
Which are Ondansetron Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- ONDANSETRON HYDROCHLORIDE (UNII: NMH84OZK2B)
- ONDANSETRON (UNII: 4AF302ESOS) (Active Moiety)
Which are Ondansetron 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:
- LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)
- POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
- STARCH, CORN (UNII: O8232NY3SJ)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
What is the NDC to RxNorm Crosswalk for Ondansetron Hydrochloride?
- RxCUI: 198052 - ondansetron HCl 4 MG Oral Tablet
- RxCUI: 198052 - ondansetron 4 MG Oral Tablet
- RxCUI: 198052 - ondansetron 4 MG (as ondansetron HCl dihydrate 5 MG) Oral Tablet
- RxCUI: 312084 - ondansetron 24 MG Oral Tablet
- RxCUI: 312084 - ondansetron 24 MG (ondansetron hydrochloride dihydrate 30 MG) Oral Tablet
Which are the Pharmacologic Classes for Ondansetron Hydrochloride?
* Please review the disclaimer below.
Patient Education
Ondansetron
Ondansetron is used to prevent nausea and vomiting caused by cancer chemotherapy, radiation therapy, and surgery. Ondansetron is in a class of medications called serotonin 5-HT3 receptor antagonists. It works by blocking the action of serotonin, a natural substance that may cause nausea and vomiting.
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* Please review the disclaimer below.
[1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
[2] What is the Substance Name? - An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
[3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
[4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[6] What is the FDA Application Number? - This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
[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".