NDC 68151-1281 Desmopressin Acetate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68151 - Carilion Materials Management
- 68151-1281 - Desmopressin Acetate
Product Characteristics
Product Packages
NDC Code 68151-1281-0
Package Description: 1 TABLET in 1 PACKAGE
Product Details
What is NDC 68151-1281?
What are the uses for Desmopressin Acetate?
Which are Desmopressin Acetate UNII Codes?
The UNII codes for the active ingredients in this product are:
- DESMOPRESSIN ACETATE (UNII: XB13HYU18U)
- DESMOPRESSIN (UNII: ENR1LLB0FP) (Active Moiety)
Which are Desmopressin Acetate 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:
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- POVIDONE K30 (UNII: U725QWY32X)
- STARCH, CORN (UNII: O8232NY3SJ)
What is the NDC to RxNorm Crosswalk for Desmopressin Acetate?
- RxCUI: 849515 - desmopressin acetate 0.1 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".