NDC 16590-895 Geodon
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 16590 - Stat Rx Usa Llc
- 16590-895 - Geodon
Product Characteristics
WHITE (C48325)
Product Packages
NDC Code 16590-895-30
Package Description: 30 CAPSULE in 1 BOTTLE
NDC Code 16590-895-60
Package Description: 60 CAPSULE in 1 BOTTLE
NDC Code 16590-895-90
Package Description: 90 CAPSULE in 1 BOTTLE
Product Details
What is NDC 16590-895?
What are the uses for Geodon?
Which are Geodon UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZIPRASIDONE HYDROCHLORIDE (UNII: 216X081ORU)
- ZIPRASIDONE (UNII: 6UKA5VEJ6X) (Active Moiety)
Which are Geodon 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 (UNII: J2B2A4N98G)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
What is the NDC to RxNorm Crosswalk for Geodon?
- RxCUI: 285127 - Geodon 20 MG Oral Capsule
- RxCUI: 285127 - ziprasidone 20 MG Oral Capsule [Geodon]
- RxCUI: 285127 - Geodon (as ziprasidone hydrochloride monohydrate) 20 MG Oral Capsule
- RxCUI: 314286 - ziprasidone HCl 20 MG Oral Capsule
- RxCUI: 314286 - ziprasidone 20 MG Oral Capsule
* Please review the disclaimer below.
[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".