NDC 10135-611 Oxybutynin Chloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
PINK (C48328)
WHITE (C48325)
A;32
A;33
Code Structure Chart
Product Details
What is NDC 10135-611?
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:
- METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A (UNII: NX76LV5T8J)
- HYDROGENATED COTTONSEED OIL (UNII: Z82Y2C65EA)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- TALC (UNII: 7SEV7J4R1U)
- TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- D&C RED NO. 27 (UNII: 2LRS185U6K)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
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
- RxCUI: 863628 - oxyBUTYnin chloride 15 MG 24HR Extended Release Oral Tablet
- RxCUI: 863628 - 24 HR oxybutynin chloride 15 MG Extended Release Oral Tablet
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Patient Education
Oxybutynin
Oxybutynin is used to treat overactive bladder (a condition in which the bladder muscles contract uncontrollably and cause frequent urination, urgent need to urinate, and inability to control urination) in certain adults and children. Oxybutynin is also used as an extended-release tablet to control bladder muscles in adults and children 6 years of age and older with spina bifida (a disability that occurs when the spinal cord does not close properly before birth), or other nervous system conditions that affect the bladder muscles. Oxybutynin is in a class of medications called anticholinergics/antimuscarinics. It works by relaxing the bladder muscles.
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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".