NDC 17856-1061 Diphenoxylate Hydrochloride And Atropine Sulfate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 17856 - Atlantic Biologicals Corps
- 17856-1061 - Diphenoxylate Hydrochloride And Atropine Sulfate
Product Characteristics
Product Packages
NDC Code 17856-1061-1
Package Description: 100 DOSE PACK in 1 CONTAINER / 1 TABLET in 1 DOSE PACK
Product Details
What is NDC 17856-1061?
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:
- ACACIA (UNII: 5C5403N26O)
- STARCH, CORN (UNII: O8232NY3SJ)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- SORBITOL (UNII: 506T60A25R)
- SUCROSE (UNII: C151H8M554)
- TALC (UNII: 7SEV7J4R1U)
What is the NDC to RxNorm Crosswalk for Diphenoxylate Hydrochloride And Atropine Sulfate?
- RxCUI: 1190572 - diphenoxylate HCl 2.5 MG / atropine sulfate 0.025 MG Oral Tablet
- RxCUI: 1190572 - atropine sulfate 0.025 MG / diphenoxylate hydrochloride 2.5 MG Oral Tablet
* Please review the disclaimer below.
[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".