NDC 64725-1438 Fluphenazine Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 64725 - Tya Pharmaceuticals
- 64725-1438 - Fluphenazine Hydrochloride
Product Characteristics
Product Packages
NDC Code 64725-1438-1
Package Description: 100 TABLET, FILM COATED in 1 CONTAINER
Product Details
What is NDC 64725-1438?
What are the uses for Fluphenazine Hydrochloride?
Which are Fluphenazine Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- FLUPHENAZINE HYDROCHLORIDE (UNII: ZOU145W1XL)
- FLUPHENAZINE (UNII: S79426A41Z) (Active Moiety)
Which are Fluphenazine 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)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- HYDROXYPROPYL CELLULOSE (TYPE H) (UNII: RFW2ET671P)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- HYPROMELLOSE 2910 (3 MPA.S) (UNII: 0VUT3PMY82)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- STARCH, CORN (UNII: O8232NY3SJ)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Fluphenazine Hydrochloride?
- RxCUI: 860918 - fluPHENAZine HCl 5 MG Oral Tablet
- RxCUI: 860918 - fluphenazine hydrochloride 5 MG Oral Tablet
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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".