NDC 11534-013 Bisacodyl
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 11534-013?
What are the uses for Bisacodyl?
Which are Bisacodyl UNII Codes?
The UNII codes for the active ingredients in this product are:
- BISACODYL (UNII: 10X0709Y6I)
- BISACODYL (UNII: 10X0709Y6I) (Active Moiety)
Which are Bisacodyl 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:
- CALCIUM SULFATE (UNII: WAT0DDB505)
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- GELATIN (UNII: 2G86QN327L)
- HYPROMELLOSE 2910 (5 MPA.S) (UNII: R75537T0T4)
- KAOLIN (UNII: 24H4NWX5CO)
- LACTOSE (UNII: J2B2A4N98G)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A (UNII: NX76LV5T8J)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- MINERAL OIL (UNII: T5L8T28FGP)
- POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- SUCROSE (UNII: C151H8M554)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
What is the NDC to RxNorm Crosswalk for Bisacodyl?
- RxCUI: 308753 - bisacodyl 5 MG Delayed Release Oral Tablet
- RxCUI: 308753 - bisacodyl 5 MG Enteric Coated 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".