NDC 64679-991 Ziprasidone Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 64679 - Wockhardt Usa Llc.
- 64679-991 - Ziprasidone Hydrochloride
Product Characteristics
WHITE (C48325 - BODY)
Product Packages
NDC Code 64679-991-01
Package Description: 30 CAPSULE in 1 BOTTLE
NDC Code 64679-991-03
Package Description: 100 CAPSULE in 1 BOTTLE
NDC Code 64679-991-06
Package Description: 10 BLISTER PACK in 1 CARTON / 8 CAPSULE in 1 BLISTER PACK
Product Details
What is NDC 64679-991?
What are the uses for Ziprasidone Hydrochloride?
Which are Ziprasidone Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZIPRASIDONE HYDROCHLORIDE (UNII: 216X081ORU)
- ZIPRASIDONE (UNII: 6UKA5VEJ6X) (Active Moiety)
Which are Ziprasidone 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:
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- GELATIN (UNII: 2G86QN327L)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Ziprasidone Hydrochloride?
- RxCUI: 313776 - ziprasidone HCl 40 MG Oral Capsule
- RxCUI: 313776 - ziprasidone 40 MG Oral Capsule
- RxCUI: 313776 - ziprasidone (as ziprasidone hydrochloride monohydrate) 40 MG Oral Capsule
- RxCUI: 313777 - ziprasidone HCl 60 MG Oral Capsule
- RxCUI: 313777 - ziprasidone 60 MG Oral Capsule
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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".