NDC 64725-0993 Ziprasidone Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 64725 - Tya Pharmaceuticals
- 64725-0993 - Ziprasidone Hydrochloride
Product Characteristics
BLUE (C48333 - BODY)
PINK (C48328 - CAP)
WHITE (C48325 - BODY)
18 MM
W993
Product Packages
NDC Code 64725-0993-1
Package Description: 60 CAPSULE in 1 BOTTLE
Product Details
What is NDC 64725-0993?
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)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C RED NO. 3 (UNII: PN2ZH5LOQY)
- 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)
- D&C RED NO. 28 (UNII: 767IP0Y5NH)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
What is the NDC to RxNorm Crosswalk for Ziprasidone Hydrochloride?
- RxCUI: 313777 - ziprasidone HCl 60 MG Oral Capsule
- RxCUI: 313777 - ziprasidone 60 MG Oral Capsule
- RxCUI: 313777 - ziprasidone (as ziprasidone HCl monohydrate) 60 MG Oral Capsule
- RxCUI: 313778 - ziprasidone HCl 80 MG Oral Capsule
- RxCUI: 313778 - ziprasidone 80 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".