NDC 53808-0819 Trifluoperazine Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 53808 - State Of Florida Doh Central Pharmacy
- 53808-0819 - Trifluoperazine Hydrochloride
Product Characteristics
PURPLE (C48327 - LAVENDER)
10 MM
M;T6
Product Packages
NDC Code 53808-0819-1
Package Description: 30 TABLET, FILM COATED in 1 BLISTER PACK
Product Details
What is NDC 53808-0819?
What are the uses for Trifluoperazine Hydrochloride?
Which are Trifluoperazine Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- TRIFLUOPERAZINE HYDROCHLORIDE (UNII: 6P1Y2SNF5V)
- TRIFLUOPERAZINE (UNII: 214IZI85K3) (Active Moiety)
Which are Trifluoperazine 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:
- COLLOIDAL SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- POLYDEXTROSE (UNII: VH2XOU12IE)
- POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)
- STARCH, CORN (UNII: O8232NY3SJ)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TRIACETIN (UNII: XHX3C3X673)
- D&C RED NO. 30 (UNII: 2S42T2808B)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
What is the NDC to RxNorm Crosswalk for Trifluoperazine Hydrochloride?
- RxCUI: 198323 - trifluoperazine HCl 10 MG Oral Tablet
- RxCUI: 198323 - trifluoperazine 10 MG Oral Tablet
- RxCUI: 198323 - trifluoperazine (as trifluoperazine hydrochloride) 10 MG Oral Tablet
- RxCUI: 198324 - trifluoperazine HCl 2 MG Oral Tablet
- RxCUI: 198324 - trifluoperazine 2 MG Oral Tablet
* 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".