NDC 17856-3194 Diphenoxylate Hydrochloride And Atropine Sulfate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 17856 - Atlantic Biologicals Corps
- 17856-3194 - Diphenoxylate Hydrochloride And Atropine Sulfate
Product Characteristics
Product Packages
NDC Code 17856-3194-5
Package Description: 72 CUP in 1 BOX / 5 mL in 1 CUP
Product Details
What is NDC 17856-3194?
What are the uses for Diphenoxylate Hydrochloride And Atropine Sulfate?
Which are Diphenoxylate Hydrochloride And Atropine Sulfate UNII Codes?
The UNII codes for the active ingredients in this product are:
- DIPHENOXYLATE HYDROCHLORIDE (UNII: W24OD7YW48)
- DIPHENOXYLATE (UNII: 73312P173G) (Active Moiety)
- ATROPINE SULFATE (UNII: 03J5ZE7KA5)
- ATROPINE (UNII: 7C0697DR9I) (Active Moiety)
Which are Diphenoxylate Hydrochloride And Atropine Sulfate 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:
- ALCOHOL (UNII: 3K9958V90M)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- GLYCERIN (UNII: PDC6A3C0OX)
- MALTOL (UNII: 3A9RD92BS4)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- SORBITOL (UNII: 506T60A25R)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Diphenoxylate Hydrochloride And Atropine Sulfate?
- RxCUI: 1190568 - atropine sulfate 0.025 MG / diphenoxylate HCl 2.5 MG in 5 mL Oral Solution
- RxCUI: 1190568 - atropine sulfate 0.005 MG/ML / diphenoxylate hydrochloride 0.5 MG/ML Oral Solution
- RxCUI: 1190568 - atropine sulfate 0.025 MG / diphenoxylate HCl 2.5 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".