NDC 53217-335 Oxybutynin Chloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 53217 - Aidarex Pharmaceuticals Llc
- 53217-335 - Oxybutynin Chloride
Product Characteristics
Product Packages
NDC Code 53217-335-30
Package Description: 30 TABLET in 1 BOTTLE
Product Details
What is NDC 53217-335?
What are the uses for Oxybutynin Chloride?
Which are Oxybutynin Chloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- OXYBUTYNIN CHLORIDE (UNII: L9F3D9RENQ)
- OXYBUTYNIN (UNII: K9P6MC7092) (Active Moiety)
Which are Oxybutynin Chloride 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)
- CALCIUM STEARATE (UNII: 776XM7047L)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
What is the NDC to RxNorm Crosswalk for Oxybutynin Chloride?
- RxCUI: 863664 - oxyBUTYnin chloride 5 MG Oral Tablet
- RxCUI: 863664 - oxybutynin chloride 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".