NDC 54868-2803 Transderm Scop
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 54868-2803?
What are the uses for Transderm Scop?
Which are Transderm Scop UNII Codes?
The UNII codes for the active ingredients in this product are:
- SCOPOLAMINE (UNII: DL48G20X8X)
- SCOPOLAMINE (UNII: DL48G20X8X) (Active Moiety)
Which are Transderm Scop 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:
- POLYISOBUTYLENE (1100000 MW) (UNII: FLT10CH37X)
- POLYISOBUTYLENE (35000 MW) (UNII: 98553S1MHQ)
- LIGHT MINERAL OIL (UNII: N6K5787QVP)
- CHLOROFORM (UNII: 7V31YC746X)
What is the NDC to RxNorm Crosswalk for Transderm Scop?
- RxCUI: 226552 - scopolamine 1 MG 3 Day Transdermal System
- RxCUI: 226552 - 72 HR scopolamine 0.0139 MG/HR Transdermal System
- RxCUI: 226552 - scopolamine 0.0139 MG/HR 72 HR Transdermal Patch
- RxCUI: 226552 - scopolamine 0.3336 MG/Day 72 HR Transdermal Patch
- RxCUI: 226552 - scopolamine 1.3 MG 3 Day Transdermal System
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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".