NDC 58118-7927 Bisacodyl Enteric Coated
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 58118 - Clinical Solutions Wholesale
- 58118-7927 - Bisacodyl
Product Characteristics
Product Packages
NDC Code 58118-7927-0
Package Description: 1 TABLET, COATED in 1 PACKAGE
NDC Code 58118-7927-3
Package Description: 30 TABLET, COATED in 1 BOTTLE
NDC Code 58118-7927-6
Package Description: 60 TABLET, COATED in 1 BOTTLE
NDC Code 58118-7927-8
Package Description: 30 TABLET, COATED in 1 BLISTER PACK
NDC Code 58118-7927-9
Package Description: 90 TABLET, COATED in 1 BOTTLE
Product Details
What is NDC 58118-7927?
What are the uses for Bisacodyl Enteric Coated?
Which are Bisacodyl Enteric Coated UNII Codes?
The UNII codes for the active ingredients in this product are:
- BISACODYL (UNII: 10X0709Y6I)
- BISACODYL (UNII: 10X0709Y6I) (Active Moiety)
Which are Bisacodyl Enteric Coated 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)
- CALCIUM SULFATE ANHYDROUS (UNII: E934B3V59H)
- ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- STARCH, CORN (UNII: O8232NY3SJ)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- GELATIN (UNII: 2G86QN327L)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- AMMONIUM NONOXYNOL-4 SULFATE (UNII: 9HIA70O4J0)
- SHELLAC (UNII: 46N107B71O)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- POLYVINYL ACETATE PHTHALATE (UNII: 58QVG85GW3)
What is the NDC to RxNorm Crosswalk for Bisacodyl Enteric Coated?
- 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".