NDC 60219-1678 Fluphenazine Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 60219 - Amneal Pharmaceuticals Ny Llc
- 60219-1678 - Fluphenazine Hydrochloride
Product Characteristics
Product Packages
NDC Code 60219-1678-1
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Price per Unit: $0.22720 per EA
Product Details
What is NDC 60219-1678?
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:
- ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)
- HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH)
- HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Fluphenazine Hydrochloride?
- RxCUI: 859841 - fluPHENAZine HCl 10 MG Oral Tablet
- RxCUI: 859841 - fluphenazine hydrochloride 10 MG Oral Tablet
- RxCUI: 860918 - fluPHENAZine HCl 5 MG Oral Tablet
- RxCUI: 860918 - fluphenazine hydrochloride 5 MG Oral Tablet
- RxCUI: 865117 - fluPHENAZine HCl 1 MG Oral Tablet
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Patient Education
Fluphenazine
Fluphenazine is an antipsychotic medication used to treat schizophrenia and psychotic symptoms such as hallucinations, delusions, and hostility. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.
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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".