NDC 68151-9200 Oxybutynin Chloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68151 - Carilion Materials Management
- 68151-9200 - Oxybutynin Chloride
Product Characteristics
GREEN (C48329)
Product Packages
NDC Code 68151-9200-1
Package Description: 5 mL in 1 SYRINGE, PLASTIC
Product Details
What is NDC 68151-9200?
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:
- WATER (UNII: 059QF0KO0R)
- TRISODIUM CITRATE DIHYDRATE (UNII: B22547B95K)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- SUCROSE (UNII: C151H8M554)
- SORBITOL (UNII: 506T60A25R)
- GLYCERIN (UNII: PDC6A3C0OX)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
What is the NDC to RxNorm Crosswalk for Oxybutynin Chloride?
- RxCUI: 863599 - oxyBUTYnin chloride 5 MG in 5 mL Oral Solution
- RxCUI: 863599 - oxybutynin chloride 1 MG/ML Oral Solution
- RxCUI: 863599 - oxybutynin chloride 5 MG per 5 ML Oral Solution
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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".