NDC 43353-769 Oxybutynin Chloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 43353-769?
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)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MANNITOL (UNII: 3OWL53L36A)
- ANHYDROUS DEXTROSE (UNII: 5SL0G7R0OK)
- TARTARIC ACID (UNII: W4888I119H)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE ACETATE (UNII: 3J2P07GVB6)
- POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TRIACETIN (UNII: XHX3C3X673)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
What is the NDC to RxNorm Crosswalk for Oxybutynin Chloride?
- RxCUI: 863619 - oxyBUTYnin chloride 10 MG 24HR Extended Release Oral Tablet
- RxCUI: 863619 - 24 HR oxybutynin chloride 10 MG Extended Release Oral Tablet
- RxCUI: 863619 - oxybutynin chloride 10 MG 24 HR Extended Release 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".