NDC 50090-2994 Trihexyphenidyl Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50090 - A-s Medication Solutions
- 50090-2994 - Trihexyphenidyl Hydrochloride
Product Characteristics
Product Packages
NDC Code 50090-2994-0
Package Description: 32 BLISTER PACK in 1 BOX, UNIT-DOSE / 1 TABLET in 1 BLISTER PACK
Product Details
What is NDC 50090-2994?
What are the uses for Trihexyphenidyl Hydrochloride?
Which are Trihexyphenidyl Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- TRIHEXYPHENIDYL HYDROCHLORIDE (UNII: AO61G82577)
- TRIHEXYPHENIDYL (UNII: 6RC5V8B7PO) (Active Moiety)
Which are Trihexyphenidyl 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:
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- ANHYDROUS DIBASIC CALCIUM PHOSPHATE (UNII: L11K75P92J)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
What is the NDC to RxNorm Crosswalk for Trihexyphenidyl Hydrochloride?
- RxCUI: 905269 - trihexyphenidyl HCl 2 MG Oral Tablet
- RxCUI: 905269 - trihexyphenidyl hydrochloride 2 MG Oral Tablet
* Please review the disclaimer below.
Patient Education
Trihexyphenidyl
Trihexyphenidyl is used along with other medications to treat the symptoms of Parkinson's disease (PD; a disorder of the nervous system that causes difficulties with movement, muscle control, and balance) and to control extrapyramidal symptoms (tremor, slurred speech) caused by certain medications. Trihexyphenidyl is in a class of medications called antimuscarinics. It works by relaxing muscles and nerve impulses that control the function of muscles.
[Learn More]
* 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".