NDC 55648-727 Ondansetron Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 55648 - Wockhardt Limited
- 55648-727 - Ondansetron Hydrochloride
Product Packages
NDC Code 55648-727-01
Package Description: 1 VIAL, MULTI-DOSE in 1 CARTON / 20 mL in 1 VIAL, MULTI-DOSE
Product Details
What is NDC 55648-727?
What are the uses for Ondansetron Hydrochloride?
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:
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- TRISODIUM CITRATE DIHYDRATE (UNII: B22547B95K)
- WATER (UNII: 059QF0KO0R)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
What is the NDC to RxNorm Crosswalk for Ondansetron Hydrochloride?
- RxCUI: 1740467 - ondansetron 4 MG in 2 ML Injection
- RxCUI: 1740467 - 2 ML ondansetron 2 MG/ML Injection
- RxCUI: 1740467 - ondansetron 4 MG per 2 ML Injection
- RxCUI: 283504 - ondansetron 2 MG/ML Injectable Solution
- RxCUI: 283504 - ondansetron (as ondansetron HCl ) 2 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".