NDC 50090-3882 Benztropine Mesylate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50090 - A-s Medication Solutions
- 50090-3882 - Benztropine Mesylate
Product Characteristics
Product Packages
NDC Code 50090-3882-0
Package Description: 30 TABLET in 1 BOTTLE
Product Details
What is NDC 50090-3882?
What are the uses for Benztropine Mesylate?
Which are Benztropine Mesylate UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZTROPINE MESYLATE (UNII: WMJ8TL7510)
- BENZTROPINE (UNII: 1NHL2J4X8K) (Active Moiety)
Which are Benztropine Mesylate 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 DIBASIC CALCIUM PHOSPHATE (UNII: L11K75P92J)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- STARCH, CORN (UNII: O8232NY3SJ)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)
- TALC (UNII: 7SEV7J4R1U)
- CORN OIL (UNII: 8470G57WFM)
What is the NDC to RxNorm Crosswalk for Benztropine Mesylate?
- RxCUI: 885209 - benztropine mesylate 2 MG Oral Tablet
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Patient Education
Benztropine
Benztropine 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 tremors caused by other medical problems or medications. Benztropine is in a class of medications called anticholinergics. It works by blocking a certain natural substance (acetylcholine) to help to decrease symptoms in people with Parkinson's disease.
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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".