NDC 64725-2168 Ziprasidone Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
BLUE (C48333 - OPAQUE BLUE BODY)
19 MM
SZ;659
Code Structure Chart
Product Details
What is NDC 64725-2168?
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:
- CALCIUM SILICATE (UNII: S4255P4G5M)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- STARCH, CORN (UNII: O8232NY3SJ)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- GELATIN (UNII: 2G86QN327L)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SHELLAC (UNII: 46N107B71O)
- AMMONIA (UNII: 5138Q19F1X)
- CARBOXYMETHYLCELLULOSE (UNII: 05JZI7B19X)
What is the NDC to RxNorm Crosswalk for Ziprasidone Hydrochloride?
- RxCUI: 313778 - ziprasidone HCl 80 MG Oral Capsule
- RxCUI: 313778 - ziprasidone 80 MG Oral Capsule
- RxCUI: 313778 - ziprasidone (as ziprasidone hydrochloride monohydrate) 80 MG Oral Capsule
- RxCUI: 314286 - ziprasidone HCl 20 MG Oral Capsule
- RxCUI: 314286 - ziprasidone 20 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".