NDC 33261-749 Senexon-s
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 33261 - Aidarex Pharmaceuticals Llc
- 33261-749 - Senexon-s
Product Characteristics
Product Packages
NDC Code 33261-749-00
Package Description: 100 TABLET, COATED in 1 BOTTLE, PLASTIC
Product Details
What is NDC 33261-749?
Which are Senexon-s UNII Codes?
The UNII codes for the active ingredients in this product are:
- DOCUSATE SODIUM (UNII: F05Q2T2JA0)
- DOCUSATE (UNII: M7P27195AG) (Active Moiety)
- SENNOSIDES A AND B (UNII: 1B5FPI42EN)
- SENNOSIDES A AND B (UNII: 1B5FPI42EN) (Active Moiety)
Which are Senexon-s 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:
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- CALCIUM PHOSPHATE, DIBASIC, DIHYDRATE (UNII: O7TSZ97GEP)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- HYPROMELLOSE 2910 (6 MPA.S) (UNII: 0WZ8WG20P6)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Senexon-s?
- RxCUI: 1248013 - Senexon-S 50 MG / 8.6 MG Oral Tablet
- RxCUI: 1248013 - docusate sodium 50 MG / sennosides, USP 8.6 MG Oral Tablet [Senexon S]
- RxCUI: 1248013 - DOSS Sodium 50 MG / sennosides, USP 8.6 MG Oral Tablet [Senexon S]
- RxCUI: 1248013 - Senexon-S (docusate sodium 50 MG / sennosides, USP 8.6 MG) Oral Tablet
- RxCUI: 998740 - sennosides 8.6 MG / docusate sodium 50 MG 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".